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| - | {{:Team:Paris_Bettencourt/Wiki}}
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| - | {{:Team:Paris_Bettencourt/Menu}}
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| - | <html>
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| | | | |
| - | <img src="https://static.igem.org/mediawiki/2013/3/3e/PB_notebookbanner.png"/>
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| - | <?php
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| - | header("X-XSS-Protection: 0");
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| - | ?>
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| - | <script type="text/javascript" src="https://2012.igem.org/Team:Paris_Bettencourt/js/RunOnLoad.js?action=raw&ctype=text/javascript"></script>
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| - | <script type="text/javascript" src="https://2012.igem.org/Team:Paris_Bettencourt/js/CollapsibleLists?action=raw&ctype=text/javascript"></script>
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| - | <script type="text/javascript">
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| - | runOnLoad(function(){ CollapsibleLists.apply(); });
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| - | </script>
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| - |
| |
| - | <style type="text/css">
| |
| - | /* CSS Tree menu styles */
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| - | #page #leftscroll li::before, #page #leftscroll li li::before {
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| - | content: "";
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| - | }
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| - | #page #leftscroll li li {
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| - | padding-left:1.5em;
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| - | }
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| - | #page #leftscroll li {
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| - | margin:0;
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| - | padding:0;
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| - | cursor: auto;
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| - | }
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| - | .treeView{
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| - | -moz-user-select:none;
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| - | position:relative;
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| - | list-style-type: none;
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| - | text-decoration: none;
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| - | }
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| - | .treeView ul{
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| - | margin:0 0 0 -1.5em;
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| - | padding:0 0 0 1.5em;
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| - | }
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| - | .treeView ul ul{
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| - | }
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| - | .treeView li.lastChild > ul{
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| - | background-image:none;
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| - | }
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| - | .treeView li{
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| - | margin:0;
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| - | padding:0;
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| - | list-style-position:inside;
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| - | list-style-image:url('https://static.igem.org/mediawiki/2013/1/17/PB_CL_Button.png');
| |
| - | cursor:auto;
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| - | }
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| - | .treeView li.collapsibleListOpen{
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| - | list-style-image:url('https://static.igem.org/mediawiki/2013/4/4a/PB_CL_Button-open.png');
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| - | cursor:pointer;
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| - | }
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| - | .treeView li.collapsibleListClosed{
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| - | list-style-image:url('https://static.igem.org/mediawiki/2013/3/3b/PB_CL_Button-closed.png');
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| - | cursor:pointer;
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| - | }
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| - | .treeView li li{
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| - | padding-left:1.5em;
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| - | }
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| - | .treeView li.lastChild{
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| - | }
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| - | .treeView li.collapsibleListOpen{
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| - | }
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| - | .treeView li.collapsibleListOpen.lastChild{
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| - | }
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| - |
| |
| - | #leftscroll{
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| - | float: left;
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| - | width: 330px;;
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| - | height: 800px;
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| - | overflow-x: scroll;
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| - | overflow-y: scroll;
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| - | overflow: scroll;
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| - | display:display;
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| - | font-size:17px;
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| - | }
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| - |
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| - | #rightscroll{
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| - | /*display: inline;*/
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| - | margin-left:32%;
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| - | width: 748px;
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| - | height: 800px;
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| - | overflow-x: scroll;
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| - | overflow-y: scroll;
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| - | overflow: scroll;
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| - | }
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| - |
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| - | .tbnote {
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| - | width: 95%;
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| - | margin-left:2.5%;
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| - | /*overflow: auto;
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| - | overflow-x: auto;
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| - | overflow-y: auto;*/
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| - | text-align:justify;
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| - | }
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| - | .tbnote h2 {
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| - | float:left;
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| - | width: 85%;
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| - | }
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| - | .tbnotelogo {
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| - | float:right;
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| - | display:block;
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| - | height:60px;
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| - | width:60px;
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| - | text-indent:100%;
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| - | white-space:nowrap;
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| - | target:blank;
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| - | background-size:60px 60px;
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| - | }
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| - | .DSlogo {
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| - | background-image:url('https://static.igem.org/mediawiki/2013/1/11/PB_TargetIcon.gif');
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| - | }
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| - | .PSlogo {
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| - | width:40px;
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| - | background-size:40px 60px;
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| - | background-image:url('https://static.igem.org/mediawiki/2013/0/0b/PB_detecticon.gif');
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| - | }
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| - | .THlogo {
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| - | background-image:url('https://2013.igem.org/Team:Paris_Bettencourt/Project/Sabotage');
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| - | }
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| - | .TClogo {
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| - | background-image:url('https://static.igem.org/mediawiki/2013/6/6c/PB_infiltrate.gif');
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| - | }
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| - | </style>
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| - |
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| - | <div id="page">
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| - | <div id="leftscroll">
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| - | <ul class="treeView">
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| - | <li>
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| - | DAY NOTES
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| - | <ul class=" collapsibleList">
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| - | <li class=" collapsibleListClosed">
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| - | DETECT
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| - | <ul style="display: none;">
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| - | <li class=" collapsibleList">
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| - | July
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| - | <ul style="display: none;">
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| - | <li class=""><a href="#detect_Saturday_13th_July.html"> Saturday 13<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#detect_Sunday_14th_July.html"> Sunday 14<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#detect_Monday_15th_July.html"> Monday 15<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#detect_Tuesday_16th_July.html"> Tuesday 16<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#detect_Wednesday_17th_July.html"> Wednesday 17<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#detect_Thursday_18th_July.html"> Thursday 18<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#detect_Monday_22nd_July.html"> Monday 22<sup>nd</sup> July</a></li>
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| - | <li class=""><a href="#detect_Tuesday_23rd_July.html"> Tuesday 23<sup>rd</sup> July</a></li>
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| - | <li class=""><a href="#detect_Monday_29th_July.html"> Monday 29<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#detect_Tuesday_30th_July.html"> Tuesday 30<sup>th</sup> July</a></li>
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| - | <li class="lastChild"><a href="#detect_Wednesday_31st_July.html"> Wednesday 31<sup>st</sup> July</a></li>
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| - | </ul>
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| - | </li>
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| - | <li class=" collapsibleList">
| |
| - | August
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| - | <ul style="display: none;">
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| - | <li class=""><a href="#detect_Thursday_1st_August.html"> Thursday 1<sup>st</sup> August</a></li>
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| - | <li class=""><a href="#detect_Friday_2nd_August.html"> Friday 2<sup>nd</sup> August</a></li>
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| - | <li class=""><a href="#detect_Monday_5th_August.html"> Monday 5<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Tuesday_6th_August.html"> Tuesday 6<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Wednesday_7th_August.html"> Wednesday 7<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Thursday_8th_August.html"> Thursday 8<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Friday_9th_August.html"> Friday 9<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Saturday_10th_August.html"> Saturday 10<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Sunday_11th_August.html"> Sunday 11<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Monday_12th_August.html"> Monday 12<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Tuesday_13th_August.html"> Tuesday 13<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Wednesday_14th_August.html"> Wednesday 14<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Thursday_15th_August.html"> Thursday 15<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Friday_16th_August.html"> Friday 16<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Monday_19th_August.html"> Monday 19<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Tuesday_20th_August.html"> Tuesday 20<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Wednesday_21st_August.html"> Wednesday 21<sup>st</sup> August</a></li>
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| - | <li class=""><a href="#detect_Thursday_22nd_August.html"> Thursday 22<sup>nd</sup> August</a></li>
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| - | <li class=""><a href="#detect_Friday_23rd_August.html"> Friday 23<sup>rd</sup> August</a></li>
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| - | <li class=""><a href="#detect_Sunday_25th_August.html"> Sunday 25<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Monday_26th_August.html"> Monday 26<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Tuesday_27th_August.html"> Tuesday 27<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#detect_Wednesday_28th_August.html"> Wednesday 28<sup>th</sup> August</a></li>
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| - | <li class="lastChild"><a href="#detect_Friday_30th_August.html"> Friday 30<sup>th</sup> August</a></li>
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| - | </ul>
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| - | </li>
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| - | <li class=" collapsibleList">
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| - | September
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| - | <ul style="display: none;">
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| - | <li class=""><a href="#detect_Tuesday_3rd_September.html"> Tuesday 3<sup>rd</sup> September</a></li>
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| - | <li class=""><a href="#detect_Wednesday_4th_September.html"> Wednesday 4<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Thursday_5th_September.html"> Thursday 5<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Friday_6th_September.html"> Friday 6<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Saturday_7th_September.html"> Saturday 7<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Sunday_8th_September.html"> Sunday 8<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Monday_16th_September.html"> Monday 16<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Tuesday_17th_September.html"> Tuesday 17<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Wednesday_18th_September.html"> Wednesday 18<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Sunday_22nd_September.html"> Sunday 22<sup>nd</sup> September</a></li>
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| - | <li class=""><a href="#detect_Monday_23rd_September.html"> Monday 23<sup>rd</sup> September</a></li>
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| - | <li class=""><a href="#detect_Tuesday_24th_September.html"> Tuesday 24<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Wednesday_25th_September.html"> Wednesday 25<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Thursday_26th_September.html"> Thursday 26<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Friday_27th_September.html"> Friday 27<sup>th</sup> September</a></li>
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| - | <li class=""><a href="#detect_Saturday_28th_September.html"> Saturday 28<sup>th</sup> September</a></li>
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| - | <li class="lastChild"><a href="#detect_Monday_30th_September.html"> Monday 30<sup>th</sup> September</a></li>
| |
| - | </ul>
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| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | October
| |
| - | <ul style="display: none;">
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| - | <li class=""><a href="#detect_Tuesday_1st_October.html"> Tuesday 1<sup>st</sup> October</a></li>
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| - | <li class=""><a href="#detect_Wednesday_2nd_October.html"> Wednesday 2<sup>nd</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Thursday_3rd_October.html"> Thursday 3<sup>rd</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Monday_14th_October.html"> Monday 14<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Tuesday_15th_October.html"> Tuesday 15<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Wednesday_16th_October.html"> Wednesday 16<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Thursday_17th_October.html"> Thursday 17<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Friday_18th_October.html"> Friday 18<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Saturday_19th_October.html"> Saturday 19<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Tuesday_22nd_October.html"> Tuesday 22<sup>nd</sup> October</a></li>
| |
| - | <li class=""><a href="#detect_Thursday_24th_October.html"> Thursday 24<sup>th</sup> October</a></li>
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| - | <li class="lastChild"><a href="#detect_Friday_25th_October.html"> Friday 25<sup>th</sup> October</a></li>
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| - | </ul>
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| - | </li>
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| - | </ul>
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| - | </li>
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| - | <li class=" collapsibleListClosed">
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| - | TARGET
| |
| - | <ul style="display: none;">
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| - | <li class=" collapsibleList">
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| - | June
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| - | <ul style="display: none;">
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| - | <li class=""><a href="#target_Monday_10th_June.html"> Monday 10<sup>th</sup> June</a></li>
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| - | <li class=""><a href="#target_Tuesday_11th_June.html"> Tuesday 11<sup>th</sup> June</a></li>
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| - | <li class=""><a href="#target_Wednesday_12th_June.html"> Wednesday 12<sup>th</sup> June</a></li>
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| - | <li class=""><a href="#target_Tuesday_18th_June.html"> Tuesday 18<sup>th</sup> June</a></li>
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| - | <li class="lastChild"><a href="#target_Monday_24th_June.html"> Monday 24<sup>th</sup> June</a></li>
| |
| - | </ul>
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| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | July
| |
| - | <ul style="display: none;">
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| - | <li class=""><a href="#target_Monday_1st_July.html"> Monday 1<sup>st</sup> July</a></li>
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| - | <li class=""><a href="#target_Tuesday_2nd_July.html"> Tuesday 2<sup>nd</sup> July</a></li>
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| - | <li class=""><a href="#target_Wednesday_3rd_July.html"> Wednesday 3<sup>rd</sup> July</a></li>
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| - | <li class=""><a href="#target_Thursday_4th_July.html"> Thursday 4<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#target_Friday_5th_July.html"> Friday 5<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#target_Tuesday_16th_July.html"> Tuesday 16<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#target_Wednesday_17th_July.html"> Wednesday 17<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#target_Thursday_18th_July.html"> Thursday 18<sup>th</sup> July</a></li>
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| - | <li class=""><a href="#target_Friday_19th_July.html"> Friday 19<sup>th</sup> July</a></li>
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| - | <li class="lastChild"><a href="#target_Wednesday_24th_July.html"> Wednesday 24<sup>th</sup> July</a></li>
| |
| - | </ul>
| |
| - | </li>
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| - | <li class=" collapsibleList">
| |
| - | August
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| - | <ul style="display: none;">
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| - | <li class=""><a href="#target_Monday_5th_August.html"> Monday 5<sup>th</sup> August</a></li>
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| - | <li class=""><a href="#target_Tuesday_6th_August.html"> Tuesday 6<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Monday_19th_August.html"> Monday 19<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Tuesday_20th_August.html"> Tuesday 20<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Wednesday_21st_August.html"> Wednesday 21<sup>st</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Thursday_22nd_August.html"> Thursday 22<sup>nd</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Friday_23rd_August.html"> Friday 23<sup>rd</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Saturday_24th_August.html"> Saturday 24<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Sunday_25th_August.html"> Sunday 25<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Monday_26th_August.html"> Monday 26<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Tuesday_27th_August.html"> Tuesday 27<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Wednesday_28th_August.html"> Wednesday 28<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#target_Thursday_29th_August.html"> Thursday 29<sup>th</sup> August</a></li>
| |
| - | <li class="lastChild"><a href="#target_Friday_30th_August.html"> Friday 30<sup>th</sup> August</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | September
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#target_Monday_9th_September.html"> Monday 9<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Tuesday_10th_September.html"> Tuesday 10<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Monday_16th_September.html"> Monday 16<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Tuesday_17th_September.html"> Tuesday 17<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Wednesday_18th_September.html"> Wednesday 18<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Thursday_19th_September.html"> Thursday 19<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Saturday_21st_September.html"> Saturday 21<sup>st</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Sunday_22nd_September.html"> Sunday 22<sup>nd</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Friday_27th_September.html"> Friday 27<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Saturday_28th_September.html"> Saturday 28<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#target_Sunday_29th_September.html"> Sunday 29<sup>th</sup> September</a></li>
| |
| - | <li class="lastChild"><a href="#target_Monday_30th_September.html"> Monday 30<sup>th</sup> September</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | October
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#target_Tuesday_1st_October.html"> Tuesday 1<sup>st</sup> October</a></li>
| |
| - | <li class=""><a href="#target_Wednesday_2nd_October.html"> Wednesday 2<sup>nd</sup> October</a></li>
| |
| - | <li class="lastChild"><a href="#target_Thursday_3rd_October.html"> Thursday 3<sup>rd</sup> October</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleListClosed">
| |
| - | INFILTRATE
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| - | <ul style="display: none;">
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| - | <li class=" collapsibleList">
| |
| - | July
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#infiltrate_Monday_22nd_July.html"> Monday 22<sup>nd</sup> July</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_23rd_July.html"> Tuesday 23<sup>rd</sup> July</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_24th_July.html"> Wednesday 24<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#infiltrate_Thursday_25th_July.html"> Thursday 25<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#infiltrate_Friday_26th_July.html"> Friday 26<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#infiltrate_Monday_29th_July.html"> Monday 29<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_30th_July.html"> Tuesday 30<sup>th</sup> July</a></li>
| |
| - | <li class="lastChild"><a href="#infiltrate_Wednesday_31st_July.html"> Wednesday 31<sup>st</sup> July</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | August
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#infiltrate_Thursday_1st_August.html"> Thursday 1<sup>st</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Friday_2nd_August.html"> Friday 2<sup>nd</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Monday_5th_August.html"> Monday 5<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_6th_August.html"> Tuesday 6<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_7th_August.html"> Wednesday 7<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Thursday_8th_August.html"> Thursday 8<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Monday_12th_August.html"> Monday 12<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_13th_August.html"> Tuesday 13<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_14th_August.html"> Wednesday 14<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Thursday_15th_August.html"> Thursday 15<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Friday_16th_August.html"> Friday 16<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Saturday_17th_August.html"> Saturday 17<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Sunday_18th_August.html"> Sunday 18<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Monday_19th_August.html"> Monday 19<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_20th_August.html"> Tuesday 20<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_21st_August.html"> Wednesday 21<sup>st</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Thursday_22nd_August.html"> Thursday 22<sup>nd</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Monday_26th_August.html"> Monday 26<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_27th_August.html"> Tuesday 27<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_28th_August.html"> Wednesday 28<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Thursday_29th_August.html"> Thursday 29<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#infiltrate_Friday_30th_August.html"> Friday 30<sup>th</sup> August</a></li>
| |
| - | <li class="lastChild"><a href="#infiltrate_Saturday_31st_August.html"> Saturday 31<sup>st</sup> August</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | September
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#infiltrate_Monday_2nd_September.html"> Monday 2<sup>nd</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_3rd_September.html"> Tuesday 3<sup>rd</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_4th_September.html"> Wednesday 4<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Thursday_5th_September.html"> Thursday 5<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Friday_6th_September.html"> Friday 6<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Saturday_7th_September.html"> Saturday 7<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Monday_9th_September.html"> Monday 9<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_10th_September.html"> Tuesday 10<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_11th_September.html"> Wednesday 11<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Thursday_12th_September.html"> Thursday 12<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Friday_13th_September.html"> Friday 13<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Saturday_14th_September.html"> Saturday 14<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Sunday_15th_September.html"> Sunday 15<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Monday_16th_September.html"> Monday 16<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_17th_September.html"> Tuesday 17<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_18th_September.html"> Wednesday 18<sup>th</sup> September</a></li>
| |
| - | <li class="lastChild"><a href="#infiltrate_Friday_20th_September.html"> Friday 20<sup>th</sup> September</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | October
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#infiltrate_Tuesday_15th_October.html"> Tuesday 15<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#infiltrate_Wednesday_16th_October.html"> Wednesday 16<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#infiltrate_Thursday_17th_October.html"> Thursday 17<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#infiltrate_Friday_18th_October.html"> Friday 18<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#infiltrate_Saturday_19th_October.html"> Saturday 19<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#infiltrate_Sunday_20th_October.html"> Sunday 20<sup>th</sup> October</a></li>
| |
| - | <li class=""><a href="#infiltrate_Monday_21st_October.html"> Monday 21<sup>st</sup> October</a></li>
| |
| - | <li class=""><a href="#infiltrate_Tuesday_22nd_October.html"> Tuesday 22<sup>nd</sup> October</a></li>
| |
| - | <li class="lastChild"><a href="#infiltrate_Saturday_26th_October.html"> Saturday 26<sup>th</sup> October</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleListClosed">
| |
| - | SABOTAGE
| |
| - | <ul style="display: none;">
| |
| - | <li class=" collapsibleList">
| |
| - | June
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#sabotage_Monday_24th_June.html"> Monday 24<sup>th</sup> June</a></li>
| |
| - | <li class=""><a href="#sabotage_Tuesday_25th_June.html"> Tuesday 25<sup>th</sup> June</a></li>
| |
| - | <li class="lastChild"><a href="#sabotage_Friday_28th_June.html"> Friday 28<sup>th</sup> June</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | July
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#sabotage_Tuesday_2nd_July.html"> Tuesday 2<sup>nd</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_3rd_July.html"> Wednesday 3<sup>rd</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Thursday_4th_July.html"> Thursday 4<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Monday_15th_July.html"> Monday 15<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Tuesday_16th_July.html"> Tuesday 16<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_17th_July.html"> Wednesday 17<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Thursday_18th_July.html"> Thursday 18<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Friday_19th_July.html"> Friday 19<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Saturday_20th_July.html"> Saturday 20<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Monday_22nd_July.html"> Monday 22<sup>nd</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Tuesday_23rd_July.html"> Tuesday 23<sup>rd</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_24th_July.html"> Wednesday 24<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Thursday_25th_July.html"> Thursday 25<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Friday_26th_July.html"> Friday 26<sup>th</sup> July</a></li>
| |
| - | <li class=""><a href="#sabotage_Tuesday_30th_July.html"> Tuesday 30<sup>th</sup> July</a></li>
| |
| - | <li class="lastChild"><a href="#sabotage_Wednesday_31st_July.html"> Wednesday 31<sup>st</sup> July</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | August
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#sabotage_Thursday_1st_August.html"> Thursday 1<sup>st</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Monday_12th_August.html"> Monday 12<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Tuesday_13th_August.html"> Tuesday 13<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_14th_August.html"> Wednesday 14<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Thursday_15th_August.html"> Thursday 15<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Friday_16th_August.html"> Friday 16<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Saturday_17th_August.html"> Saturday 17<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Monday_19th_August.html"> Monday 19<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Tuesday_20th_August.html"> Tuesday 20<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_21st_August.html"> Wednesday 21<sup>st</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Thursday_22nd_August.html"> Thursday 22<sup>nd</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Friday_23rd_August.html"> Friday 23<sup>rd</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Monday_26th_August.html"> Monday 26<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Tuesday_27th_August.html"> Tuesday 27<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_28th_August.html"> Wednesday 28<sup>th</sup> August</a></li>
| |
| - | <li class=""><a href="#sabotage_Thursday_29th_August.html"> Thursday 29<sup>th</sup> August</a></li>
| |
| - | <li class="lastChild"><a href="#sabotage_Friday_30th_August.html"> Friday 30<sup>th</sup> August</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | <li class=" collapsibleList">
| |
| - | September
| |
| - | <ul style="display: none;">
| |
| - | <li class=""><a href="#sabotage_Tuesday_3rd_September.html"> Tuesday 3<sup>rd</sup> September</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_4th_September.html"> Wednesday 4<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#sabotage_Thursday_5th_September.html"> Thursday 5<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#sabotage_Saturday_7th_September.html"> Saturday 7<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#sabotage_Tuesday_10th_September.html"> Tuesday 10<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_11th_September.html"> Wednesday 11<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#sabotage_Saturday_14th_September.html"> Saturday 14<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#sabotage_Sunday_15th_September.html"> Sunday 15<sup>th</sup> September</a></li>
| |
| - | <li class=""><a href="#sabotage_Wednesday_18th_September.html"> Wednesday 18<sup>th</sup> September</a></li>
| |
| - | <li class="lastChild"><a href="#sabotage_Friday_20th_September.html"> Friday 20<sup>th</sup> September</a></li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | </ul>
| |
| - | </li>
| |
| - | </ul>
| |
| - | </div>
| |
| - | <div id="rightscroll">
| |
| - |
| |
| - | <html><div id="detect_Saturday_13th_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Saturday 13<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | PCR circular and linear, Conjugation of XL-10 (with sSP011), Patches, Digestion M13 backbone, RFP insert, Gel of PCR
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>PCR circular and linear, 40.5°C, 60°</b>
| |
| - | of pSB1A3, pSB1C3<br>
| |
| - | <br>
| |
| - | <TABLE BORDER>
| |
| - | <TR><TD><b>Reagent</b></TD><TD><b>Volume</b></TD></TR>
| |
| - | <TR><TD></TD><TD><b>1x</b></TD></TR>
| |
| - | <TR><TD>Nuclease-free water</TD><TD>37.25 ul</TD></TR>
| |
| - | <TR><TD>5x Phusion HF Buffer</TD><TD>10 ul</TD></TR>
| |
| - | <TR><TD>10 mM dNTPs</TD><TD>1 ul</TD></TR>
| |
| - | <TR><TD>Forward Primer (10 uM)</TD><TD>0.5 ul</TD></TR>
| |
| - | <TR><TD>Reverse Primer (10 uM)</TD><TD>0.5 ul</TD></TR>
| |
| - | <TR><TD>Template Plasmid</TD><TD>0.25 ul</TD></TR>
| |
| - | <TR><TD>Phusion DNA Polymerase</TD><TD>0.5 ul</TD></TR>
| |
| - | <TR><TD><b>Total Volume</b></TD><TD>50 ul</TD></TR>
| |
| - | </TABLE><br>
| |
| - | <br>
| |
| - | <TABLE BORDER>
| |
| - | <TR><TD><b>Thermocycler Protocol: NEB Phusion</b></TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD>Temp</TD><TD>Time</TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Start</TD><TD>98°C</TD><TD>30 sec</TD><TD>Melt</TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Cycle 1</TD><TD>98°C</TD><TD>5 sec</TD><TD>Melt</TD><TD> 35 cycles </TD></TR>
| |
| - | <TR><TD>Cycle 2</TD><TD>40.5°C / 60°C </TD><TD>25 sec</TD><TD>Anneal</TD><TD></TD></TR>
| |
| - | <TR><TD>Cycle 3</TD><TD>72°C</TD><TD>5 min</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Finish</TD><TD>72°C</TD><TD>5 min</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - | <TR><TD>Store</TD><TD>10°C</TD><TD>Forever</TD><TD>Store</TD><TD> </TD></TR>
| |
| - | </TABLE><br>
| |
| - | <br>
| |
| - |
| |
| - | <b>Conjugation of XL-10 (with sSP011)</b><br>
| |
| - | 1) From O/N cultures Dilute strains 1/100 in LB<br>
| |
| - | 2) Wait for OD to reach O,2<br>
| |
| - | 3) Prepare tube (in BD tubes) :<br>
| |
| - | - Tube = 0,5mL LB with Strain (sSP011) + 0,5mL LB with Strain (XL-10 Kan)<br>
| |
| - | 4) Incubate 2 hours at 37°C (actually not in the shaker, but we accidently kept them in the shaker...)<br>
| |
| - | 5) Plate 20ul for mixed tube on LB antiobiotics (Tet, Kan)<br>
| |
| - | 6) Incubate overnight at 37°C<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Patches</b><br>
| |
| - | check and make new ones<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Digestion M13 backbone, RFP insert</b><br>
| |
| - | for Backbone (M13mp18 plasmid): 3ug<br>
| |
| - | 7,58 ul plasmid (c=395ng/ul)<br>
| |
| - | 3 ul EcoRI<br>
| |
| - | 3 ul PstI<br>
| |
| - | 3ul 10x Fast Digest<br>
| |
| - | 13,42 ul H20<br>
| |
| - | incubate for 12 min on 37°<br>
| |
| - | heat inactivation: 80° 5 min<br>
| |
| - | for insert (BBa_J04450): 5ug<br>
| |
| - | 31,4 ul plasmid<br>
| |
| - | 5 ul EcoRi<br>
| |
| - | 5 ul PstI<br>
| |
| - | 3,6 ul H20<br>
| |
| - | incubate for 20 min at 37°<br>
| |
| - | heat inactivation: 80° 5min<br>
| |
| - | <br>
| |
| - | <b>Gel of PCR </b> (Amp 40.5 circ, lin, Chl 60° lin, circ)<br>
| |
| - | 100V, 20 min 1% gel<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Sunday_14th_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Sunday 14<sup>th</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel of PCR, Gel Extraction, DpnI digest of PCR products and PCR purification
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Gel of PCR</b> (Amp 60° circ, lin, Chl 40.5 circ, lin)<br>
| |
| - | 100V, 20 min 1% gel<br>
| |
| - | <br>
| |
| - | <b>Gel of Digest</b><br>
| |
| - | 100V, 20 min 1% gel<br>
| |
| - | <br>
| |
| - | <b>Gel Extraction</b><br>
| |
| - | Excise the DNA fragment from the agarose gel with a clean, sharp scalpel. Minimize the size of the gel slice by removing extra agarose.<br>
| |
| - | Weigh the gel slice in a colorless tube. Add 3 volumes of Buffer QG to 1 volume of gel (100 mg ~ 100 μl). To help dissolve gel, mix by vortexing the tube every 2–3 min during the incubation.
| |
| - | After the gel slice has dissolved completely, check that the color of the mixture is yellow (similar to Buffer QG without dissolved agarose).<br>
| |
| - | Add 1 gel volume of isopropanol to the sample and mix (actually only needed for very small products or very big products)<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column, and centrifuge for 1 min.<br>
| |
| - | Discard flow-through and place QIAquick column back in the same collection tube.<br>
| |
| - | To wash, add 0.75 ml of Buffer PE to QIAquick column and centrifuge for 1 min.<br>
| |
| - | 11. Discard the flow-through and centrifuge the QIAquick column for an additional 1 min at 17,900 x g (13,000 rpm).
| |
| - | 12. Place QIAquick column into a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 30 μl elution buffer to the center of the QIAquick membrane, let the column stand for 1 min, and then centrifuge for 1 min.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>DpnI digest of PCR products</b>:<br>
| |
| - | SPCR4 (40ul) - add 1 ul DpnI<br>
| |
| - | SPCR 7 (150ul) - add 3 ul of DpnI<br>
| |
| - | SPCR8 (60 ul) - add 3 ul of DpnI<br>
| |
| - | SPCR 9 (150ul) - add 3 ul of DpnI<br>
| |
| - | SPCR10 (110ul) - add 3 ul of DpnI<br>
| |
| - | Incubate for 15 min at 37°C<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>PCR purification</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 50 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Monday_15th_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 15<sup>th</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Plating and control of antibiotic resistance.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | We made a 1:1000 dilution of KAN (stand.c) in an LB solid media.<br>
| |
| - | <br>
| |
| - | Pouring the plates. Around 20 mL/plate<br>
| |
| - | 1. KEIOΔPYR KANR Growth<br>
| |
| - | 2. ME1655 KANR No growth<br>
| |
| - | <br>
| |
| - | Conclusion : <br>
| |
| - | <br>
| |
| - | The KEIOΔPYRF growed as expected. Negative control did not growth.<br>
| |
| - | Plates have KAN antibiotic<br>
| |
| - | KEIO has KAN R.<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_16th_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 16<sup>th</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | We prepared a colony PCR to send the KAN for sequencing, to know exactly the sequence of the KAN.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | KEIOΔMPYRF has a deletion of PYRF to be replaced by KAN<br>
| |
| - | We pitched 4 singles colonies into 50µL of H2O<br>
| |
| - | Boil 5 minutes at 95°C<br>
| |
| - | 1,5 µL of this can be used directly for PCR<br>
| |
| - | <br>
| |
| - | PCR reaction<br>
| |
| - | Keep all the regents at 4°C while preparing the mixture<br>
| |
| - | <br>
| |
| - | <table border>
| |
| - | <TR><TD>Reagent</TD><TD>Volume</TD></TR>
| |
| - | <TR><TD>JW 182 (10 uM)<br>
| |
| - | JW 183 (10 uM)<br>
| |
| - | Template DNA<br>
| |
| - | Quick-load Tag 2x Master Mix<br>
| |
| - | Nuclease free water</TD><TD>0,5 µL<br>
| |
| - | 0,5 µL<br>
| |
| - | 1,5 µL<br>
| |
| - | 12,5 µL<br>
| |
| - | 10 µL</TD></TR>
| |
| - | <TR><TD>Total volume</TD><TD>25 µL</TD></TR>
| |
| - | </TABLE><br>
| |
| - | <br>
| |
| - | Thermocycler Protocol : NEB Quick-Load<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> Temperature </td>
| |
| - | <td> Time </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start<br>
| |
| - | <br>
| |
| - | Cycle1<br>
| |
| - | Cycle 2<br>
| |
| - | Cycle 3<br>
| |
| - | <br>
| |
| - | Finish<br>
| |
| - | Store</td>
| |
| - | <td>95°C<br>
| |
| - | <br>
| |
| - | 95°C<br>
| |
| - | 50°C<br>
| |
| - | 68°C<br>
| |
| - | <br>
| |
| - | 68°C<br>
| |
| - | 10°C</td>
| |
| - | <td>30 seconds<br>
| |
| - | <br>
| |
| - | 15 seconds<br>
| |
| - | 30 seconds<br>
| |
| - | 1 minute/kB<br>
| |
| - | <br>
| |
| - | 5 minutes<br>
| |
| - | Forever</td>
| |
| - | <td>melt<br>
| |
| - | <br>
| |
| - | melt<br>
| |
| - | anneal<br>
| |
| - | extend - 35 cycles<br>
| |
| - | <br>
| |
| - | extend<br>
| |
| - | store</td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | Gel electrophoresis<br>
| |
| - | <br>
| |
| - | We do it to prove that our colony PCR was successful. We expect a band at about 800 base pairs.<br>
| |
| - | Our gel is 1%, therefore we used 0,5g agarose in 100µL TAE buffer.<br>
| |
| - | As a ladder, we used a 1kB plus gene ruler of fermentor. <br>
| |
| - | We l the gel with 5 µL sample ans we kept the sample at 4°C.<br>
| |
| - | <br>
| |
| - | PICTURE<br>
| |
| - | <br>
| |
| - | We see that the band are as expected. THis is an indicator that KAN is at the right place. The sequence has then been sent for sequencing<br>
| |
| - | <br>
| |
| - | Transformation of PAUC 18 into a NEBΔturbo clearing cells<br>
| |
| - | We are transforming PAUC 18 that consist in a low ORI and ampicillin resistance<br>
| |
| - | We will use commercialized NEB turbo competent cells as well as freshly made chemical competent cells<br>
| |
| - | We did this to check the competency of our fresh competent cells<br>
| |
| - | <br>
| |
| - | NOTE : EVERYTHING HAS TO BE KEPT ON ICE AND NO VORTEX<br>
| |
| - | <br>
| |
| - | Throw competent cells on ice. Those can be prepared using the CaCl2 protocol<br>
| |
| - | Place 20 µL of cells in a pre-chilled Eppendorf tube<br>
| |
| - | For an intert vector, add 0,5 µL or less to the chilled cells<br>
| |
| - | For a ligation product, add 2-3 µL to the chilled cells<br>
| |
| - | Mix gently by flicking the tube<br>
| |
| - | Chill on ice for 10 minutes - this step is optional but can improve yields when transforming a ligation product<br>
| |
| - | Heat shock at 42°C for 30 seconds<br>
| |
| - | Return on ice for 2 minutes<br>
| |
| - | Add 200µL LB medium and recover the cells by shaking at 37°C<br>
| |
| - | Another rich medium can substitute for the recovery. The recovery time varies with the antibiotic selection<br>
| |
| - | Ampicillin : 15 - 30 minutes<br>
| |
| - | <br>
| |
| - | Place out the cells on selective LB<br>
| |
| - | Use glass beads to spread the cells. The volume of cells plated depends on what is being transformed<br>
| |
| - | <br>
| |
| - | For an intact vector<br>
| |
| - | High transformation efficiencies are expected. Plating out 10 µL of recovered cells should produce many colonies.<br>
| |
| - | <br>
| |
| - | Note : 200 µL is the maximum volume of liquid that an LB plate can absorb<br>
| |
| - | Incubate at 37°C. Transformants should appear within 12 hours<br>
| |
| - | <br>
| |
| - | Conclusion<br>
| |
| - | The BL 21 DE3 strain showed IP colonies<br>
| |
| - | For the new NEB turbo cells, we see no colony<br>
| |
| - | The old NEB turbo cells worked fine<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_17th_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 17<sup>th</sup> of July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | PCR purification
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | We are purifying the colony PCR from yesterday to send it away for sequencing<br>
| |
| - | <br>
| |
| - | Procedure<br>
| |
| - | Add 1.1 volume and Binding Buffer<br>
| |
| - | Transfer up to 800 µL. Centrifuge for 30-60 seconds. Descend the flow through<br>
| |
| - | Add 700 µL of washed Buffer. Centrifuge for 30-60 seconds<br>
| |
| - | + 1 min centrifuge to completely remove any residual wash buffer<br>
| |
| - | Add 50 µL of Elution Buffer to the center of the Gene JT purification column membrane and centrifuge for 1 minute<br>
| |
| - | Discard the Gene JET purification column and store the purified DNA at -20°C. <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Thursday_18th_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 18<sup>th</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Calculating the transformation efficiency for the E.coli NEB and E.coli NNEB strains.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | · 20 µL of cell culture was inoculated in 200 µL of LB, where 0.5 µL of DNA sample (?) was added, giving the total volume of 220.5 µL.<br>
| |
| - | · After the heat shock transformation 10 µL of the culture was diluted in 90 µL of LB, giving the 10-1 dilution (d); then 10 µL of this dilution was transferred in 90 µL of LB, giving the 10-2 dilution. 10 µL of each dilution (v) was plated on ampicillin media and left for incubation (24 h, 37 ̊C).<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | · After incubation, colonies were counted:
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> NEB </td>
| |
| - | <td> NNEB </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> 10<sup>-¹</sup> </td>
| |
| - | <td> 0 </td>
| |
| - | <td> 433 </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> 0 </td>
| |
| - | <td> 368 </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> Average </td>
| |
| - | <td> 0 </td>
| |
| - | <td> <b>400.5<b> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> 10<sup>-¹</sup> </td>
| |
| - | <td> 0 </td>
| |
| - | <td> 62 </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> 0 </td>
| |
| - | <td> 40 </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> Average </td>
| |
| - | <td> 0 </td>
| |
| - | <td> <b>51<b> </td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | Obviously, NEB strain was not transformed and only NNEB was included in further calculations.<br>
| |
| - | · The number of the transformed colony forming units per mL of the culture was calculated following the formula: colony number / d*v.<br>
| |
| - | <br>
| |
| - | Calculation from the 10-1 dilution: 0.4 * 109 CFU/mL<br>
| |
| - | Calculation from the 10-2 dilution: 0.51 * 109 CFU/mL<br>
| |
| - | <br>
| |
| - | · The transformation efficiency was calculated by dividing the number of transformed colony forming units (CFU) by the amount of the DNA used (mDNA).<br>
| |
| - | <br>
| |
| - | CFU1 = 0.4 * 109 CFU/mL * 0.22 mL (total V of the transformation culture) = 0.088*109 CFU<br>
| |
| - | CFU2 = 0.51 * 109 CFU/mL * 0.22 mL = 0.1122*109 CFU<br>
| |
| - | <br>
| |
| - | The concentration of the DNA solution which was used was 0.323 µg/µL, while the total DNA mass which was added to the transformation culture was: 0.323 µg/µL * 0.5 µL = 0.1615 µg.<br>
| |
| - | <br>
| |
| - | So the transformation efficiency, calculated from the 10 times diluted (TE1) and 100 times diluted (TE2) cultures is:<br>
| |
| - | <br>
| |
| - | TE1 = CFU1/mDNA = 0.55 * 109 CFU/µg<br>
| |
| - | TE2 = CFU2/mDNA = 0.69 * 109 CFU/µg<br>
| |
| - | <br>
| |
| - | TE1 and TE2 are almost the same<br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Monday_22nd_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 22<sup>nd</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Culture purification by streak plate method and preparing the glycerol stock for the sSP001 (TN 57) and sSP002 (NEC) strains.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | Place your note here
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_23rd_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 23<sup>rd</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Colony PCR
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | · Strain: Keio ΔpyrF<br>
| |
| - | · Primers: JW182 and JW183<br>
| |
| - | · Amplified region: kanamycine resistance gene<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/b/b3/13%EF%80%A207%EF%80%A224_first_run_KanR.jpg"heigh=150><br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/9/91/13%EF%80%A207%EF%80%A224_second_run_KanR.jpg"heigh=200><br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Monday_29th_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 29<sup>th</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | Liquid culture of:<br>
| |
| - | pCOLA DUET (from glycerol stock of Sabotage Group) - 20 ml culture<br>
| |
| - | pSSB1 (from plate) - 5 ml culture<br>
| |
| - | pSSB2 (from plate ) - 5 ml culture<br>
| |
| - | <br>
| |
| - | Plating of addgene bacteria containing the plasmids we want:<br>
| |
| - | streak out bacteria from addgene to get single colonies:<br>
| |
| - | pBAC-BA-lacZ<br>
| |
| - | pCRISPR<br>
| |
| - | pCas9<br>
| |
| - | pCRIPSR::rpsL<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_30th_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 30<sup>th</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Liquid culture, Miniprep and Glycerol stock
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Liquid culture of:</b><br>
| |
| - | pCOLA DUET (from liquid culture (29.07.13)) - 20 ml culture<br>
| |
| - | pSSB1 (from liquid culture (29.07.13)) - 5ml culture<br>
| |
| - | pSSB2 (from liquid culture (29.07.13)) - 5 ml culture<br>
| |
| - | pBAC-BA-lacZ (from plate ) - 5 ml culture<br>
| |
| - | pCRISPR (from plate ) - 5 ml culture<br>
| |
| - | pCas9 (from plate ) - 5 ml culture<br>
| |
| - | pCRIPSR::rpsL (from plate ) - 5 ml culture<br>
| |
| - | F+ strain - (from glycerol stock Sabotage) - 10 ml culture<br>
| |
| - | Keio Keio delta pyrF (from plate ) - 10 ml culture<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Miniprep (pCOLA-DUET = sSP007) using the Thermo Scientific Miniprep Kit</b> <br>
| |
| - | <br>
| |
| - | 1) Pellet 2x9 ml of liquid culture (4000 rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250 µL of resuspension solution<br>
| |
| - | 4) add 250 µL of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350 µL of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 µL wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5 ml tube<br>
| |
| - | 11) add 50 µL of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | pSP001= pCOLA-DUET: 65 ng/ul<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Glycerol Stock</b> <br>
| |
| - | from overnight culture of MG1655-pCOLA-DUET (sSP007)<br>
| |
| - | Centrifuge 4000 rpm, 10 minutes,<br>
| |
| - | take out liquid<br>
| |
| - | resuspend cells in 0,5 mL glycerol (60%) , 2 mL LB<br>
| |
| - | freeze in -80°C<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_31st_July.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 31<sup>st</sup> July</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Conjugation, Miniprep addgene plasmids,Glycerol Stock of addgene plasmids
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <br><br>
| |
| - | <b>Conjugation</b><br>
| |
| - | <br>
| |
| - | sSP001, SP002, keio Delta PyrF<br>
| |
| - | F+ comes from XL1 Blue (glycerol stock Sabotage) => F+ is tetR<br>
| |
| - | <br>
| |
| - | Protocol :<br>
| |
| - | 1) From O/N cultures Dilute strains 1/100 in LB<br>
| |
| - | 2) Wait for OD to reach O,2<br>
| |
| - | 3) Prepare 4 tubes (in BD tubes) :<br>
| |
| - | - Tube 1 = 0,5 mL LB with Strain 1 (sSP001) ,5 mL LB = control<br>
| |
| - | - Tube 2 = 0,5 mL LB with Strain 2 (sP001) + 0,5 mL LB = control<br>
| |
| - | - Tube 3 = 0,5 mL LB with Strain 3 (keio Delta pyrF) + 0,5 mL LB = control<br>
| |
| - | - Tube 4 = 0,5 mL LB with Strain 4 (XL1) + 0,5 mL LB = control<br>
| |
| - | - Tube 5 = 0,5 mL LB with Strain 1 (sSP001) + 0,5 mL LB with Strain 4 (XL1)<br>
| |
| - | - Tube 6 = 0,5 mL LB with Strain 2 (sSP002) + 0,5 mL LB with Strain 4 (XL1)<br>
| |
| - | - Tube 7 = 0,5 mL LB with Strain 3 (keio Delta pyrF) + 0,5 mL LB with Strain 4 (XL1)<br>
| |
| - | 4) Incubate 2 hours at 37°C (actually not in the shaker, but we accidently kept them in the shaker...)<br>
| |
| - | 5) Plate 10ul for controls, 100uL, 10ul for mixed tubes on LB antibiotics (Tube 5: Chl + Tet, Tube 6: Chl + Tet, Tube 7: Kan + Tet)<br>
| |
| - | 6) Incubate overnight at 37°C<br>
| |
| - | <br>
| |
| - | <b>Miniprep addgene plasmids</b><br>
| |
| - | 1) Pellet 4 ml of liquid culture (4000 rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250 µL of resuspension solution<br>
| |
| - | 4) add 250 µL of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350 µL of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 µL wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove leftover liquid<br>
| |
| - | 10) transfer the column on a 1.5 ml tube<br>
| |
| - | 11) add 50 µL of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | See Database for plasmid reference<br>
| |
| - | pCas9: <br>
| |
| - | pCRISPR:<br>
| |
| - | pBac-LacZ:<br>
| |
| - | pCRISPR::rpsL:<br>
| |
| - | <br>
| |
| - | <b>Glycerol Stock of addgene plasmids</b><br> (see Database for strain reference)<br>
| |
| - | from overnight culture<br>
| |
| - | Centrifuge 4000 rpm, 10 minutes,<br>
| |
| - | take out liquid<br>
| |
| - | resuspend cells in 0,5 mL glycerol (60%) , 2 mL LB<br>
| |
| - | freeze in -80°C<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Thursday_1st_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 1<sup>st</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | PCR (gradient + usual) of SPCR1, SPCR7, SPCR8, SPCR10, SPCR9, SPCR4
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <TABLE BORDER>
| |
| - | <TR><TD><b>Reagent</b></TD><TD><b>Volume</b></TD></TR>
| |
| - | <TR><TD> </TD><TD><b>1x</b></TD></TR>
| |
| - | <TR><TD>Nuclease-free water</TD><TD>37.25 µL</TD></TR>
| |
| - | <TR><TD>5x Phusion HF Buffer</TD><TD>10 µL</TD></TR>
| |
| - | <TR><TD>10 mM dNTPs</TD><TD>1 µL</TD></TR>
| |
| - | <TR><TD>Forward Primer (10 µM)</TD><TD>0.5 µL</TD></TR>
| |
| - | <TR><TD>Reverse Primer (10 µM)</TD><TD>0.5 µL</TD></TR>
| |
| - | <TR><TD>Template Plasmid</TD><TD>0.25 µL</TD></TR>
| |
| - | <TR><TD>Phusion DNA Polymerase</TD><TD>0.5 µL</TD></TR>
| |
| - | <TR><TD><b>Total Volume</b></TD><TD>50 µL</TD></TR>
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - | Gradient:<br>
| |
| - | Pos 1: 40°<br>
| |
| - | Pos 2: 40,2°<br>
| |
| - | Pos 3: 41,3°<br>
| |
| - | Pos 4: 43,1°<br>
| |
| - | Pos 5: 45,4°<br>
| |
| - | Pos 6: 48°<br>
| |
| - | Pos 7: 50,7°<br>
| |
| - | Pos 8: 53,5°<br>
| |
| - | Pos 9: 56,0°<br>
| |
| - | Pos 10: 58,1°<br>
| |
| - | Pos 11: 59,8°C<br>
| |
| - | (Pos 12: 60,6°)<br>
| |
| - | <br>
| |
| - | Usual PCR: 52°<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Friday_2nd_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Friday 2<sup>nd</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Place your twit here
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gels with PCR products: 1% Agar<br>
| |
| - | 100V 20 Min<br>
| |
| - | 10 min staining in BET<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/d/d7/13%EF%80%A208%EF%80%A202_SCPR1_iS008_iS009.jpg">
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/3/3e/13%EF%80%A208%EF%80%A202_SPCR4_iS0018_iS019.jpg">
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/f/f4/13%EF%80%A208%EF%80%A202_SPCR7_iS010_iS011.jpg">
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/0/01/13%EF%80%A208%EF%80%A202_SPCR8_iS012_iS013_2.jpg">
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/f/f9/13%EF%80%A208%EF%80%A202_SPCR9_iS016_iS017.jpg">
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/f/fd/13%EF%80%A208%EF%80%A202_SPCR10_iS014_iS015.jpg">
| |
| - | <br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Saturday_3rd_August.html"</div></html>
| |
| - | <html><div id="detect_Sunday_4th_August.html"</div></html>
| |
| - | <html><div id="detect_Monday_5th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 5<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Place your twit here
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>5ml liquid culture with proper antibiotics of:</b><br>
| |
| - | SSp001 + F+<br>
| |
| - | sSP002 + F+<br>
| |
| - | keio delta pyrF + F+<br>
| |
| - | <br>
| |
| - | <b>Gelelectrophoresis:</b>
| |
| - | 1% Agar, 100 V 20 min<br>
| |
| - | <br>
| |
| - | <img src= "https://static.igem.org/mediawiki/2013/c/cf/13%EF%80%A208%EF%80%A205_SPCR7_1%2C2%2C10_SPCR4_1%2C2%2C4%2C10%2C11_SCPR10_1%2C4%2C5%2C6%2C11.jpg">
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_6th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 6<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Liquid cultures of sSP008-sSP0011
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_7th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 7<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Glycerol Stock of sSP008-sSP0011, M13 Test, Single Colonies, Liquid cultures, PCR and Transformation
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <br><b>Glycerol Stock of sSP008-sSP0011</b><br>
| |
| - | Take 1.5ml of ON culture + 500ul Glycerol (60%)<br>
| |
| - | Freeze at -80°C<br>
| |
| - | <br>
| |
| - | <b>M13 Test</b><br>
| |
| - | Plate from ON culture:<br>
| |
| - | 1) 1:1000 - sSP012: sSP009 (plate 200ul)<br>
| |
| - | 2) 200 ul sSP012<br>
| |
| - | 3) 200ul sSp009<br>
| |
| - | <br>
| |
| - | <b>Single Colonies</b><br>
| |
| - | streak out ON culture of sSP012 to get single colonies<br>
| |
| - | <br>
| |
| - | <b>Liquid cultures</b> of pir+ E.coli and pKD13 from Jake<br>
| |
| - | <br>
| |
| - | <b>PCR of SPCR4, SPCR7, SPCR8, SPCR9, SPCR10 from circuar backbone, directly taken from Biobrick plate</b><br><br>
| |
| - | Protocol<br>
| |
| - | <br>
| |
| - | <TABLE BORDER>
| |
| - | <TR><TD><b>Reagent</b></TD><TD><b>Volume</b></TD></TR>
| |
| - | <TR><TD> </TD><TD><b>1x</b></TD></TR>
| |
| - | <TR><TD>Nuclease-free water</TD><TD>37,25µL</TD></TR>
| |
| - | <TR><TD>5x Phusion HF Buffer</TD><TD>10µL</TD></TR>
| |
| - | <TR><TD>10 mM dNTPs</TD><TD>1µL</TD></TR>
| |
| - | <TR><TD>Forward Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Reverse Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Template Plasmid</TD><TD>0.25µL</TD></TR>
| |
| - | <TR><TD>Phusion DNA Polymerase</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD><b>Total Volume</b></TD><TD>50µL</TD></TR>
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - |
| |
| - | <TABLE BORDER>
| |
| - |
| |
| - | <TR><TD><b>Thermocycler Protocol: NEB Phusion</b></TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD>Temp</TD><TD>Time</TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Start</TD><TD>98°C</TD><TD>30 sec</TD><TD>Melt</TD><TD></TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Cycle 1</TD><TD>98°C</TD><TD>5 sec</TD><TD>Melt</TD><TD>35 cycles</TD></TR>
| |
| - | <TR><TD>Cycle 2</TD><TD>40.5°C / 60°C</TD><TD>25 sec</TD><TD>Anneal</TD><TD></TD></TR>
| |
| - | <TR><TD>Cycle 3</TD><TD>72°C</TD><TD>30 sec per kb</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Finish</TD><TD>72°C</TD><TD>5 min</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - |
| |
| - | <TR><TD>Store</TD><TD>10°C</TD><TD>Forever</TD><TD>Store</TD><TD></TD></TR>
| |
| - |
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - | <b>Transformation</b> Biobricks BBa_K649304 (with pSB1C3 backbone) and BBa_J04450 (with pSB1A3 backbone) into NEB Turbo (heat shock trafo)<br>
| |
| - | <br>
| |
| - | 1) Thaw competent cells on ice.<br>
| |
| - | 2) Place 20 ul of cells in a pre-chilled Eppendorf tube.<br>
| |
| - | 3) Add 2.5 ul of plasmid (from Biobrick stock)<br>
| |
| - | 4) Mix gently by flicking the tube.<br>
| |
| - | 5) Chill on ice for 10 minutes.<br>
| |
| - | 4) Heat shock at 42 °C for 30 seconds <br>
| |
| - | 5) Return to ice for 2 minutes.<br>
| |
| - | 6) Add 200 ul LB medium and recover the cells by shaking at 37 °C.<br>
| |
| - | Ampicillin: 15-30 minutes<br>
| |
| - | Chloramphenicol: 60-120 minutes<br>
| |
| - | 7) Plate out the cells on selective LB (10ul)<br>
| |
| - | 8) Incubate at 37 °C. Transformants should appear within 12 hrs.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Result</b>: BBa_J04450: many colonies, BBa_K649304 no colonies, plate rest<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Thursday_8th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 8<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Liquid culture of FR-433 (M13)
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel of PCR products. 100V 20min 1%<br>
| |
| - | <br>
| |
| - | 4-7-8-9-10 (40.5°C)- 4-7-8-9-10 (60°C)<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/f/fc/13%EF%80%A208%EF%80%A208_SPCR4_SPR7_SPCR8_SCPR9_SPCR10.jpg"<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Friday_9th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Friday 9<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Liquid culture, Gel,
| |
| - | Trafo of BBa_E1010 (pSB1C3 backbone) into NEB turbo, Glycerol Stock, Making electro competent cells of pir+ E.coli, Transforming pKD13 into pir+ E.coli, Miniprep NEB turbo with BBa-J04450:, Liquid culture and Patch plates.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <br><b>Liquid culture</b><br>
| |
| - | 1:1000 from liquid: FR-433 (M13), 10 ml<br>
| |
| - | pir+ E.coli: from plate, 25 ml<br>
| |
| - | XL10: from plate 10 ml<br>
| |
| - | <br>
| |
| - | <b>Gel</b>: rest of circular backbone PCR product, 1% Agar, 100V, 20 min<br>
| |
| - | SPCR4-7-8-9-10 (40.5) SPCR4-7-8-9-10 (60.5)<br>
| |
| - | Gel picture: <br>
| |
| - | didn’t work<br>
| |
| - | <br>
| |
| - | <b>Trafo of BBa_E1010 (pSB1C3 backbone) into NEB turbo</b><br>
| |
| - | 1) Thaw competent cells on ice.<br>
| |
| - | 2) Place 20 µl of cells in a pre-chilled Eppendorf tube.<br>
| |
| - | 3) Add 2.5 µl of plasmid (from Biobrick stock)<br>
| |
| - | 4) Mix gently by flicking the tube.<br>
| |
| - | 5) Chill on ice for 10 minutes.<br>
| |
| - | 4) Heat shock at 42 °C for 30 seconds <br>
| |
| - | 5) Return to ice for 2 minutes.<br>
| |
| - | 6) Add 200 µl LB medium and recover the cells by shaking at 37 °C.<br>
| |
| - | Chloramphenicol: 60-120 minutes<br>
| |
| - | 7) Plate out the cells on selective LB (10ul)<br>
| |
| - | 8) Incubate at 37 °C. Transformants should appear within 12 hrs.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Glycerol Stock FR-433 (M13) -> sSP012</b><br>
| |
| - | Glycerol Stock pir+ -> sSP013<br>
| |
| - | Glycerol Stock pKD13 -> sSP014<br>
| |
| - | Glycerol Stock NEB turbo with BBa-J04450 -> sSP015<br>
| |
| - | Take 1.5 ml of ON culture + 500ul Glycerol (60%)<br>
| |
| - | Freeze at -80°C<br>
| |
| - | <br>
| |
| - | <b>Making electro competent cells of pir+ E.coli</b><br>
| |
| - | Preparation of Electrocompetent Cells<br>
| |
| - | Note: Competent cells should never be vortexed, as this will cause them to lyse and release salts into the media. Resuspend cells by pipetting up and down with a large pasteur pipet. Once they are chilled, cells should be continuously cold.<br>
| |
| - | <br>
| |
| - | 1) The night before the transformation, start an overnight culture of cells.<br>
| |
| - | pir+ E.coli<br>
| |
| - | 2) The day of the transformation, dilute the cells 100X.<br>
| |
| - | 100 ml LB<br>
| |
| - | Grow at 30°C for about 90 minutes. <br>
| |
| - | 3) When the cells reach an OD600 of 0.2. <br>
| |
| - | 4) Harvest the cells.<br>
| |
| - | When the cells reach an OD600 of between 0.6 and 0.8.<br>
| |
| - | Split the culture into 2x 50 ml falcon tubes, on ice.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | 5) Wash and combine the cells.<br>
| |
| - | Remove the supernatant.<br>
| |
| - | Resuspend the cells in 2x 25 ml of ice cold water.<br>
| |
| - | Combine the volumes in a single 50 ml falcon tube.<br>
| |
| - | 6) Wash the cells 2 more times.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 50 ml of ice cold water.<br>
| |
| - | Repeat.<br>
| |
| - | 7) Wash and concentrate the cells for electroporation.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 1-2 ml of ice cold water.<br>
| |
| - | We will use 200 µl of washed cells per transformation.<br>
| |
| - | <br>
| |
| - | <b>Transforming pKD13 into pir+ E.coli</b><br>
| |
| - | 1) Prepare BD tubes with a pipette filled with LB at the interior of each tube (pipette supplied with the electroporation cuvette)<br>
| |
| - | <br>
| |
| - | 2) Test the purity of the electrocompetent cells.<br>
| |
| - | Add 200 ul of washed cells to a cuvette.<br>
| |
| - | <br>
| |
| - | 3) Mix the cells and DNA in a cuvette.<br>
| |
| - | 200 ul of washed cells with 200 ng of PCR product.<br>
| |
| - | Keep the cuvette on ice until just before the electroporation.<br>
| |
| - | <br>
| |
| - | 4) Preload a pipette with 1 ml of LB.<br>
| |
| - | <br>
| |
| - | 5) Pulse the cuvette with voltage.<br>
| |
| - | Dry the electrodes with a kimwipe prior to loading.<br>
| |
| - | Use the EC2 setting.<br>
| |
| - | <br>
| |
| - | 6) Listen for arcing.<br>
| |
| - | A cracking sound means all the cells are dead.<br>
| |
| - | Note the time constant: 5 is good, 5.8 is great.<br>
| |
| - | <br>
| |
| - | 7) Immediately recover the cells.<br>
| |
| - | Add the 1 ml of preloaded LB and pipet up and down to mix.<br>
| |
| - | Collect 1 ml of cells, some volume is lost in the cuvette.<br>
| |
| - | <br>
| |
| - | 8) Incubate 2 h at 37 °C with shaking.<br>
| |
| - | <br>
| |
| - | 9) Plate 100 ul of recovered cells on selective plates.<br>
| |
| - | Use antibiotic appropriate to the part being integrated.<br>
| |
| - | Let the other 900 ul rest overnight at room temperature.<br>
| |
| - | <br>
| |
| - | 10) Concentrate and plate the remaining cells<br>
| |
| - | Spin down quickly and resuspend in 100 ul LB before plating.<br>
| |
| - | <br>
| |
| - | Transformed cells should be incubated at 37 °C.<br>
| |
| - | Colonies should appear 24-48 h after plating.<br>
| |
| - | <br><br>
| |
| - | <b>Miniprep NEB turbo with BBa-J04450:</b><br>
| |
| - | 1) Pellet 2x 9 ml of liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250 µl of resuspension solution<br>
| |
| - | 4) add 250 µl of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350 µl of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 µl wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5 ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | J04450: 0ng/ul<br>
| |
| - | <br>
| |
| - |
| |
| - | <b>Liquid culture of:</b>
| |
| - | sSP012<br>
| |
| - | sSP008<br>
| |
| - | sSP009<br>
| |
| - | sSP010<br>
| |
| - | sSP011<br>
| |
| - | sSP001<br>
| |
| - | sSP002<br>
| |
| - | XL-10 = sSP016<br>
| |
| - | sSP017= Litmus<br>
| |
| - | <br>
| |
| - | <b>Patch plates of:</b><br>
| |
| - | sSP010<br>
| |
| - | sSP013<br>
| |
| - | sSP009s<br>
| |
| - | sSP014<br>
| |
| - | sSP012<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Saturday_10th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Saturday 10<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Test of M13 and Liquid culture
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Test of M13</b><br>
| |
| - | <br>
| |
| - | 1) 100 μ l of plating bacteria per tube<br>
| |
| - | 2) Prepare tenfold serial dilutions (10-6 to 10-9 ) of the bacteriophage stock in LB<br>
| |
| - | 3) Put 10 μ l/ 100 μ l of each dilution to the bacteria<br>
| |
| - | 4) Mix the bacteriophage particles with the bacterial culture by vortexing gently.<br>
| |
| - | 5) Add 40 μ l of X-gal solution (working conc) and IPTG (working conc) solution to each of the tubes<br>
| |
| - | 6) Add 3ml of Agar to each tube and gently vortexing for 3 seconds<br>
| |
| - | 7) Pour the mixture onto plates containing LB medium supplemented with 5 mM MgCl2 <br>
| |
| - | 8) Swirl the plate gently to ensure an even distribution of bacteria and agar.<br>
| |
| - | 9) Incubate them at 37°C.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Liquid culture:</b><br>
| |
| - | E1010<br>
| |
| - | J04550<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Sunday_11th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Sunday 11<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Patches of sSP001-sSP008, sSP015-18 and Stress experiment (Plate reader)
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Patches of sSP001-sSP008, sSP015-18</b><br>
| |
| - | <br>
| |
| - | <b>Stress experiment (Plate reader)</b><br>
| |
| - | sSP001, sSP002, sSP010, sSP011, sSP012 (M13)<br>
| |
| - | 1:1000 bacteria in M9 Glucose<br>
| |
| - | Mitomycin C concentrations: 3,3*10^-3, 1,6*10°-3, 6,6*10°-4, 3,3*10°-4<br>
| |
| - | Quadruplets of bacteria (+phage), Triplets of MMC<br>
| |
| - | <br>
| |
| - | See also pipetting scheme in folder Experiments on Dropbox<br>
| |
| - | <br>
| |
| - | <b>On culture of FR-433, XL-10, delta pyrF </b><br>
| |
| - | 1:1000 culture at 30°<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Monday_12th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 12<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Glycerol Stock, Miniprep, M13 plate test, Patches
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Glycerol Stock</b>
| |
| - | sSP018 - NEB with E1010<br>
| |
| - | sSP017<br>
| |
| - | sSP016<br>
| |
| - | Take 1.5ml of ON culture + 500ul Glycerol (60%)<br>
| |
| - | Freeze at -80°C<br>
| |
| - | <br>
| |
| - | <b>Miniprep</b><br>
| |
| - | E1010<br>
| |
| - | J04450<br>
| |
| - | <br>
| |
| - | 1) Pellet 2x 2ml of liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250ul of resuspension olution<br>
| |
| - | 4) add 250ul of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350ul of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 ul wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | J04450: ng/ul<br>
| |
| - | E1010: ng/ul<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>M13 plate test</b><br>
| |
| - | 1) 100 μ l of plating bacteria per tube<br>
| |
| - | 2) Prepare tenfold serial dilutions (10-6 to 10-9 ) of the bacteriophage stock in LB<br>
| |
| - | 3) Put 10 μ l/ 100 μ l of each dilution to the bacteria<br>
| |
| - | 4) Mix the bacteriophage particles with the bacterial culture by vortexing gently.<br>
| |
| - | 5) Add 40 μ l of X-gal solution (working conc) and IPTG (working conc) solution to each of the tubes<br>
| |
| - | 6) Add 3ml of Agar to each tube and gently vortexing for 3 seconds<br>
| |
| - | 7) Pour the mixture onto plates containing LB medium supplemented with 5 mM MgCl2 <br>
| |
| - | 8) Swirl the plate gently to ensure an even distribution of bacteria and agar.<br>
| |
| - | 9) Incubate them at 37°C.<br>
| |
| - | <br>
| |
| - | <b>Patches</b><br>
| |
| - | check them and prepare new ones of those that haven’t been done yet<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_13th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 13<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | PCR circular and linear 40.5°C/ 60°C, Conjugation of XL-10 (with sSP011), Patches, Digestion M13 backbone, RFP insert and Gel of PCR
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>PCR circular and linear, 40.5°C, 60°</b>
| |
| - | of pSB1A3, pSB1C3<br>
| |
| - | <br>
| |
| - | <TABLE BORDER>
| |
| - | <TR><TD><b>Reagent</b></TD><TD><b>Volume</b></TD></TR>
| |
| - | <TR><TD> </TD><TD><b>1x</b></TD></TR>
| |
| - | <TR><TD>Nuclease-free water</TD><TD>37,25µL</TD></TR>
| |
| - | <TR><TD>5x Phusion HF Buffer</TD><TD>10µL</TD></TR>
| |
| - | <TR><TD>10 mM dNTPs</TD><TD>1µL</TD></TR>
| |
| - | <TR><TD>Forward Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Reverse Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Template Plasmid</TD><TD>0.25µL</TD></TR>
| |
| - | <TR><TD>Phusion DNA Polymerase</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD><b>Total Volume</b></TD><TD>50µL</TD></TR>
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - |
| |
| - | <TABLE BORDER>
| |
| - |
| |
| - | <TR><TD><b>Thermocycler Protocol: NEB Phusion</b></TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD>Temp</TD><TD>Time</TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Start</TD><TD>98°C</TD><TD>30 sec</TD><TD>Melt</TD><TD></TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Cycle 1</TD><TD>98°C</TD><TD>5 sec</TD><TD>Melt</TD><TD>35 cycles</TD></TR>
| |
| - | <TR><TD>Cycle 2</TD><TD>40.5°C / 60°C</TD><TD>25 sec</TD><TD>Anneal</TD><TD></TD></TR>
| |
| - | <TR><TD>Cycle 3</TD><TD>72°C</TD><TD>30 sec per kb</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Finish</TD><TD>72°C</TD><TD>5 min</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - |
| |
| - | <TR><TD>Store</TD><TD>10°C</TD><TD>Forever</TD><TD>Store</TD><TD></TD></TR>
| |
| - |
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - | <b>Conjugation of XL-10 (with sSP011)</b><br>
| |
| - | 1) From O/N cultures Dilute strains 1/100 in LB<br>
| |
| - | 2) Wait for OD to reach O,2<br>
| |
| - | 3) Prepare tube (in BD tubes) :<br>
| |
| - | - Tube = 0,5mL LB with Strain (sSP011) + 0,5mL LB with Strain (XL-10 Kan)<br>
| |
| - | 4) Incubate 2 hours at 37°C (actually not in the shaker, but we accidently kept them in the shaker...)<br>
| |
| - | 5) Plate 20ul for mixed tube on LB antiobiotics (Tet, Kan)<br>
| |
| - | 6) Incubate overnight at 37°C<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Patches</b><br>
| |
| - | check and make new ones<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Digestion M13 backbone, RFP insert</b><br>
| |
| - | for Backbone (M13mp18 plasmid): 3ug<br>
| |
| - | 7,58 ul plasmid (c=395ng/ul)<br>
| |
| - | 3 ul EcoRI<br>
| |
| - | 3 ul PstI<br>
| |
| - | 3ul 10x Fast Digest<br>
| |
| - | 13,42 ul H20<br>
| |
| - | incubate for 12 min on 37°<br>
| |
| - | heat inactivation: 80° 5 min<br>
| |
| - | for insert (BBa_J04450): 5ug<br>
| |
| - | 31,4 ul plasmid<br>
| |
| - | 5 ul EcoRi<br>
| |
| - | 5 ul PstI<br>
| |
| - | 3,6 ul H20<br>
| |
| - | incubate for 20 min at 37°<br>
| |
| - | heat inactivation: 80° 5min<br>
| |
| - | <br>
| |
| - | <b>Gel of PCR (Amp 40.5 circ, lin, Chl 60° lin, circ)</b><br>
| |
| - | 100V, 20 min 1% gel<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/5/5d/13%EF%80%A208%EF%80%A213_SPCR_AmpR_backbones_40.5%C2%B0_60%C2%B0_circular_linear_4%2C7%2C8%2C9%2C10.jpg"height="300"><br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/2/27/13%EF%80%A208%EF%80%A213_SPCRs_ChlR_backbones_40.5%C2%B0_60%C2%B0_circular_linear_4%2C7%2C8%2C9%2C10.jpg"height="330"><br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_14th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 14<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel of PCR, Gel of Digest, Gel Extraction, DpnI digest of PCR products, PCR purification
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <b>Gel of PCR</b> (Amp 60° circ, lin, Chl 40.5 circ, lin)
| |
| - | 100V, 20 min 1% gel<br>
| |
| - | <br>
| |
| - | <b>Gel of Digest</b><br>
| |
| - | 100V, 20 min 1% gel<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/1/1a/13%EF%80%A208%EF%80%A214_SPCR_AmpR_backbones_40.5%C2%B0_60%C2%B0_circular_linear_4%2C7%2C8%2C9%2C10.jpg"><br>
| |
| - | <br>
| |
| - | <b>Gel Extraction</b><br>
| |
| - | Excise the DNA fragment from the agarose gel with a clean, sharp scalpel. Minimize the size of the gel slice by removing extra agarose.<br>
| |
| - | Weigh the gel slice in a colorless tube. Add 3 volumes of Buffer QG to 1 volume of gel (100 mg ~ 100 μl). To help dissolve gel, mix by vortexing the tube every 2–3 min during the incubation.<br>
| |
| - | After the gel slice has dissolved completely, check that the color of the mixture is yellow (similar to Buffer QG without dissolved agarose).<br>
| |
| - | Add 1 gel volume of isopropanol to the sample and mix (actually only needed for very small products or very big products)<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column, and centrifuge for 1 min.<br>
| |
| - | Discard flow-through and place QIAquick column back in the same collection tube.<br>
| |
| - | To wash, add 0.75 ml of Buffer PE to QIAquick column and centrifuge for 1 min.<br>
| |
| - | 11. Discard the flow-through and centrifuge the QIAquick column for an additional 1 min at 17,900 x g (13,000 rpm).
| |
| - | 12. Place QIAquick column into a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 30 μl elution buffer to the center of the QIAquick membrane, let the column stand for 1 min, and then centrifuge for 1 min.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>DpnI digest of PCR products:</b><br>
| |
| - | SPCR4 (40ul) - add 1 ul DpnI<br>
| |
| - | SPCR 7 (150ul) - add 3 ul of DpnI<br>
| |
| - | SPCR8 (60 ul) - add 3 ul of DpnI<br>
| |
| - | SPCR 9 (150ul) - add 3 ul of DpnI<br>
| |
| - | SPCR10 (110ul) - add 3 ul of DpnI<br>
| |
| - | Incubate for 15 min at 37°C<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>PCR purification</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 50 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Thursday_15th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 15<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Liquid cultures
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Liquid cultures</b>:<br>
| |
| - | sSp009<br>
| |
| - | sSP012<br>
| |
| - | sSP016<br>
| |
| - | sSp020<br>
| |
| - | Xgal Bacteria from Aude<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Friday_16th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Friday 16<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Liquid M13 Test, Glycerol Stock, Miniprep
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Liquid M13 Test</b><br>
| |
| - | <br>
| |
| - | OD (sSP020=XL10 KanR with F+)=0,557<br>
| |
| - | OD (sSP016=XL10 KanR)=0,515<br>
| |
| - | OD (sSP009= delta pyrF with F+)=0,561<br>
| |
| - | OD(sSP012=FR-433=M13)=0,695<br>
| |
| - | <br>
| |
| - | Prepare Falcons containing 500ul of each strain, adding 500ul of 10^-6 dilution of FR-433<br>
| |
| - | add 1ul of IPTG and 1ul of Xgal<br>
| |
| - | Incubate at 37° on shaker<br>
| |
| - | <br>
| |
| - | <b>Glycerol Stock</b>
| |
| - | sSP019 (pir+ E.coli transformed with pKD13)<br>
| |
| - | sSP020 (XL10 KanR with F+)<br>
| |
| - | <br>
| |
| - | <b>Miniprep</b><br>
| |
| - | sSP019<br>
| |
| - | sSP017<br>
| |
| - | <br>
| |
| - | 1) Pellet 2x 2ml of liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250ul of resuspension olution<br>
| |
| - | 4) add 250ul of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350ul of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 ul wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | pKD13: 311ng/ul<br>
| |
| - | Litmus 28i: 93ng/ul<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Monday_19th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 19<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Restreak XL-1 Blue Litmus28i, PCR, PCR purification Backbone (M13mp18), Ligation (RFP into M13mp18 backbone), Trafo of Ligation product (RFP in M13mp18 plasmid) into NEB turbo and Test Xgal
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Restreak XL-1 Blue Litmus28i</b><br>
| |
| - | <br>
| |
| - | <b>PCR</b><br>
| |
| - | <br>
| |
| - | SPCR5, SPCR6, 49,3°C<br>
| |
| - | <br>
| |
| - | <TABLE BORDER>
| |
| - | <TR><TD><b>Reagent</b></TD><TD><b>Volume</b></TD></TR>
| |
| - | <TR><TD> </TD><TD><b>1x</b></TD></TR>
| |
| - | <TR><TD>Nuclease-free water</TD><TD>37,25µL</TD></TR>
| |
| - | <TR><TD>5x Phusion HF Buffer</TD><TD>10µL</TD></TR>
| |
| - | <TR><TD>10 mM dNTPs</TD><TD>1µL</TD></TR>
| |
| - | <TR><TD>Forward Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Reverse Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Template Plasmid</TD><TD>0.25µL</TD></TR>
| |
| - | <TR><TD>Phusion DNA Polymerase</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD><b>Total Volume</b></TD><TD>50µL</TD></TR>
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - |
| |
| - | <TABLE BORDER>
| |
| - |
| |
| - | <TR><TD><b>Thermocycler Protocol: NEB Phusion</b></TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD>Temp</TD><TD>Time</TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Start</TD><TD>98°C</TD><TD>30 sec</TD><TD>Melt</TD><TD></TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Cycle 1</TD><TD>98°C</TD><TD>5 sec</TD><TD>Melt</TD><TD>35 cycles</TD></TR>
| |
| - | <TR><TD>Cycle 2</TD><TD>40.5°C / 60°C</TD><TD>25 sec</TD><TD>Anneal</TD><TD></TD></TR>
| |
| - | <TR><TD>Cycle 3</TD><TD>72°C</TD><TD>30 sec per kb</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Finish</TD><TD>72°C</TD><TD>5 min</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - |
| |
| - | <TR><TD>Store</TD><TD>10°C</TD><TD>Forever</TD><TD>Store</TD><TD></TD></TR>
| |
| - |
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - | <b>PCR purification Backbone (M13mp18)</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 50 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | <b>Ligation (RFP into M13mp18 backbone)</b><br>
| |
| - | 3ul Backbone<br>
| |
| - | 14 ul Insert<br>
| |
| - | 2ul 10x T4 DNA Ligase HC Buffer<br>
| |
| - | 1 ul T4 DNA Ligase<br>
| |
| - | <br>
| |
| - | Incubate for at least 10min at 22°C<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Trafo of Ligation product (RFP in M13mp18 plasmid) into NEB turbo</b><br>
| |
| - | 1) Thaw competent cells on ice.<br>
| |
| - | 2) Place 20 ul of cells in a pre-chilled Eppendorf tube.<br>
| |
| - | 3) Add 3 ul of plasmid (from Biobrick stock)<br>
| |
| - | 4) Mix gently by flicking the tube.<br>
| |
| - | 5) Chill on ice for 10 minutes.<br>
| |
| - | 4) Heat shock at 42 °C for 30 seconds <br>
| |
| - | 5) Return to ice for 2 minutes.<br>
| |
| - | 6) Add 200 ul LB medium and recover the cells by shaking at 37 °C.<br>
| |
| - | 7) Plate out the cells on LB (200ul)<br>
| |
| - | 8. Incubate at 37 °C. Transformants should appear within 12 hrs.<br>
| |
| - | <br>
| |
| - | <b>Test Xgal</b><br>
| |
| - | 3ml of Liquid culture with <br>
| |
| - | 1) Xgal from iGEM 2012 (Jake) (+IPTG)<br>
| |
| - | 2) Xgal from last week (in DMF) (+IPTG)<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_20th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 20<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel of PCR and Xgal Test
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Gel of PCR</b><br>
| |
| - | <br>
| |
| - | 1%, 100V, 20min<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/a/a2/13%EF%80%A208%EF%80%A220_at_49.3C_SPCR5_iS005_iS007_SPCR6_iS005_iS006.jpg"height="400"><br>
| |
| - | <br>
| |
| - | Result: PCR didn’t work<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Xgal Test</b><br>
| |
| - | <br>
| |
| - | MG1655 (of Jake) in liquid culture with Xgal of iGEM 2012, Aude and new one (Anne)<br>
| |
| - | <br>
| |
| - | Result:<br>
| |
| - | All cultures turn blue (Aude, less blue)<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_21st_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 21<sup>st</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gradient PCR SPCR5, SPCR6, M13 Test, Electrocompetent Cells (sSP017-XL-1 Blue, Litmus 28i), Transformation
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Gradient PCR SPCR5, SPCR6</b><br>
| |
| - | <br>
| |
| - | <TABLE BORDER>
| |
| - | <TR><TD><b>Reagent</b></TD><TD><b>Volume</b></TD></TR>
| |
| - | <TR><TD> </TD><TD><b>1x</b></TD></TR>
| |
| - | <TR><TD>Nuclease-free water</TD><TD>37,25µL</TD></TR>
| |
| - | <TR><TD>5x Phusion HF Buffer</TD><TD>10µL</TD></TR>
| |
| - | <TR><TD>10 mM dNTPs</TD><TD>1µL</TD></TR>
| |
| - | <TR><TD>Forward Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Reverse Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Template Plasmid</TD><TD>0.25µL</TD></TR>
| |
| - | <TR><TD>Phusion DNA Polymerase</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD><b>Total Volume</b></TD><TD>50µL</TD></TR>
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - | Gradient:<br>
| |
| - | Pos 1: 40.1°<br>
| |
| - | Pos 2: 40,8°<br>
| |
| - | Pos 3: 42.2°<br>
| |
| - | Pos 4: 44.2°<br>
| |
| - | Pos 5: 46.7°<br>
| |
| - | Pos 6: 49.4°<br>
| |
| - | Pos 7: 52.1°<br>
| |
| - | Pos 8: 54.7°<br>
| |
| - | Pos 9: 57.1°<br>
| |
| - | Pos 10: 59.0°<br>
| |
| - | Pos 11: 60.2°C<br>
| |
| - | <br>
| |
| - | <b>M13 Test</b><br>
| |
| - | Liquid cultures of sSP012 and sSP020<br>
| |
| - | 1) 100 μ l of plating bacteria per tube<br>
| |
| - | 2) Prepare tenfold serial dilutions (10-6 to 10-9 ) of the bacteriophage stock in LB<br>
| |
| - | 3) Put 10 μ l/ 100 μ l of each dilution to the bacteria<br>
| |
| - | 4) Mix the bacteriophage particles with the bacterial culture by vortexing gently.<br>
| |
| - | 5) Add 40 μ l of X-gal solution (working conc) and IPTG (working conc) solution to each of the tubes<br>
| |
| - | 6) Add 3ml of Agar to each tube and gently vortexing for 3 seconds<br>
| |
| - | 7) Pour the mixture onto plates containing LB medium supplemented with 5 mM MgCl2 <br>
| |
| - | 8) Swirl the plate gently to ensure an even distribution of bacteria and agar.<br>
| |
| - | 9) Incubate them at 37°C.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Electrocompetent Cells (sSP017-XL-1 Blue, Litmus 28i)</b><br>
| |
| - | 1) The night before the transformation, start an overnight culture of cells.<br>
| |
| - | sSP017 (XL1 Blue Litmus 28i)<br>
| |
| - | 2) The day of the transformation, dilute the cells 100X.<br>
| |
| - | 100 ml LB Amp.<br>
| |
| - | Grow at 30°C for about 90 minutes. <br>
| |
| - | 3) When the cells reach an OD600 of 0.2. <br>
| |
| - | 4) Harvest the cells.<br>
| |
| - | When the cells reach an OD600 of between 0.6 and 0.8 (OD: 0,683)<br>
| |
| - | Split the culture into 2x 50 ml falcon tubes, on ice.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | 5) Wash and combine the cells.<br>
| |
| - | Remove the supernatant.<br>
| |
| - | Resuspend the cells in 2x 25 ml of ice cold water.<br>
| |
| - | Combine the volumes in a single 50 ml falcon tube.<br>
| |
| - | 6) Wash the cells 2 more times.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 50 ml of ice cold water.<br>
| |
| - | Repeat.<br>
| |
| - | 7) Wash and concentrate the cells for electroporation.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 1-2 ml of ice cold water.<br>
| |
| - | We will use 200 ul of washed cells per transformation.<br>
| |
| - | <br>
| |
| - | <b>Transforming pKD13 into pir+ E.coli</b><br>
| |
| - | 1) Prepare BD tubes with a pipette filled with LB at the interior of each tube (pipette supplied with the electroporation cuvette)<br>
| |
| - | <br>
| |
| - | 2) Test the purity of the electrocompetent cells.<br>
| |
| - | Add 200 ul of washed cells to a cuvette.<br>
| |
| - | <br>
| |
| - | 3) Mix the cells and DNA in a cuvette.<br>
| |
| - | 200 ul of washed cells with 200 ng of PCR product.<br>
| |
| - | Keep the cuvette on ice until just before the electroporation.<br>
| |
| - | <br>
| |
| - | 4) Preload a pipette with 1 ml of LB.<br>
| |
| - | <br>
| |
| - | 5) Pulse the cuvette with voltage.<br>
| |
| - | Dry the electrodes with a kimwipe prior to loading.<br>
| |
| - | Use the EC2 setting.<br>
| |
| - | <br>
| |
| - | 6) Listen for arcing.<br>
| |
| - | A cracking sound means all the cells are dead.<br>
| |
| - | Note the time constant: 5 is good, 5.8 is great.<br>
| |
| - | <br>
| |
| - | 7) Immediately recover the cells.<br>
| |
| - | Add the 1 ml of preloaded LB and pipet up and down to mix.<br>
| |
| - | Collect 1 ml of cells, some volume is lost in the cuvette.<br>
| |
| - | <br>
| |
| - | 8) Incubate 2 h at 37 °C with shaking.<br>
| |
| - | <br>
| |
| - | 9) Plate 100 ul of recovered cells on selective plates.<br>
| |
| - | Use antibiotic appropriate to the part being integrated.<br>
| |
| - | Let the other 900 ul rest overnight at room temperature.<br>
| |
| - | <br>
| |
| - | 10) Concentrate and plate the remaining cells<br>
| |
| - | Spin down quickly and resuspend in 100 ul LB before plating.<br>
| |
| - | <br>
| |
| - | Transformed cells should be incubated at 37 °C.<br>
| |
| - | Colonies should appear 24-48 h after plating.<br>
| |
| - | <br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Thursday_22nd_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 22<sup>nd</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | Gel of gradient PCR product (Pictures 6,5,5), PCR purification and pooling, Digestion M13 backbone, RFP insert, Test Digestion in Gel, Gel Extraction, Liquid culture, Purification of Backbone Cloning and Miniprep sSP015.
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <br>
| |
| - | <b>Gel of gradient PCR product </b><br>
| |
| - | 1%, 100V, 20 min<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/5/56/13%EF%80%A208%EF%80%A222_Degest_BBaJ%294550_with_EcoRI_PstI.jpg"><br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/e/e8/13%EF%80%A208%EF%80%A222_SPCR_6_iS005_iS006.jpg"><br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/d/d3/13%EF%80%A208%EF%80%A222_SPCR5_iS005_iS007.jpg"><br>
| |
| - | <br>
| |
| - | <b>PCR purification and pooling</b><br>
| |
| - | Pool all samples that worked<br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 50 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | c(SPCR5)= ng/ul<br>
| |
| - | c(SPCR6)= ng/ul<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Digestion M13 backbone, RFP insert</b><br>
| |
| - | <br>
| |
| - | Backbone/Insert (double the amount)<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td>Regent</td><td>Volume</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Purified Plasmid</td><td>20 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td><td>65 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10x FastDigest Buffer</td><td>10 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 1 (EcoRI)</td><td>2,5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 2 (PstI)</td><td>2,5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastAP Phosphatase</td><td>0 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td><td><b>100ul</b></td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | Digest for 2.5 hours at 37 °C with shaking.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Test Digestion in Gel</b><br>
| |
| - | 1%, 100V, 20 min<br>
| |
| - | <br>
| |
| - | <b>Gel Extraction</b><br>
| |
| - | Excise the DNA fragment from the agarose gel with a clean, sharp scalpel. Minimize the size of the gel slice by removing extra agarose.<br>
| |
| - | Weigh the gel slice in a colorless tube. Add 3 volumes of Buffer QG to 1 volume of gel (100 mg ~ 100 μl). To help dissolve gel, mix by vortexing the tube every 2–3 min during the incubation.<br>
| |
| - | After the gel slice has dissolved completely, check that the color of the mixture is yellow (similar to Buffer QG without dissolved agarose).<br>
| |
| - | Add 1 gel volume of isopropanol to the sample and mix (actually only needed for very small products or very big products)<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column, and centrifuge for 1 min.<br>
| |
| - | Discard flow-through and place QIAquick column back in the same collection tube.<br>
| |
| - | To wash, add 0.75 ml of Buffer PE to QIAquick column and centrifuge for 1 min.<br>
| |
| - | 11. Discard the flow-through and centrifuge the QIAquick column for an additional 1 min at 17,900 x g (13,000 rpm).
| |
| - | 12. Place QIAquick column into a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 30 μl elution buffer to the center of the QIAquick membrane, let the column stand for 1 min, and then centrifuge for 1 min.<br>
| |
| - | <br>
| |
| - | c=13,6ng/ul<br>
| |
| - | <br>
| |
| - | Liquid culture<br>
| |
| - | sSP015<br>
| |
| - | <br>
| |
| - | <b>Purification of Backbone Cloning</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 30 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | <b>Miniprep sSP015</b><br>
| |
| - | 1) Pellet 2x 2ml of liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250ul of resuspension solution<br>
| |
| - | 4) add 250ul of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350ul of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 ul wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Friday_23rd_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Friday 23<sup>rd</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Stress Experiment (sSP001, sSP002, sSP010, sSP011, M13, MMC), Microscope, Gradient PCR of SPCR2, Digestion of SPCR 5 and SPCR7 and Purification of Digestion.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Stress Experiment (sSP001, sSP002, sSP010, sSP011, M13, MMC)</b><br>
| |
| - | Dilute ON culture 1:100<br>
| |
| - | Centrifuge (1 min, 10rpm)<br>
| |
| - | Wash 1x with 70% of Volume M9 Glucose<br>
| |
| - | Centrifuge again<br>
| |
| - | Take up in 70% of the VOlume M9 Gluo<br>
| |
| - | 100ul in each 96 well plate (see pipetting file)<br>
| |
| - | Add MMC 10ug/ml in corresponding wells and incubate in the plate reader<br>
| |
| - | After 90 min add phages into correscponding wells<br>
| |
| - | put back on the plate reader<br>
| |
| - | <br>
| |
| - | <b>Microscope</b><br>
| |
| - | look at the shape and fluorescence at t=0 of sSP001<br>
| |
| - | look at the shape and fluorescence at=90 mi of sSP001 + 10ug/ml MMC<br>
| |
| - | take photos<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Gradient PCR of SPCR2</b><br>
| |
| - | iSP001 (gblock) and iS002<br>
| |
| - |
| |
| - | <br>
| |
| - | <TABLE BORDER>
| |
| - | <TR><TD><b>Reagent</b></TD><TD><b>Volume</b></TD></TR>
| |
| - | <TR><TD> </TD><TD><b>1x</b></TD></TR>
| |
| - | <TR><TD>Nuclease-free water</TD><TD>37,25µL</TD></TR>
| |
| - | <TR><TD>5x Phusion HF Buffer</TD><TD>10µL</TD></TR>
| |
| - | <TR><TD>10 mM dNTPs</TD><TD>1µL</TD></TR>
| |
| - | <TR><TD>Forward Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Reverse Primer (10 µM)</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD>Template Plasmid</TD><TD>0.25µL</TD></TR>
| |
| - | <TR><TD>Phusion DNA Polymerase</TD><TD>0.5µL</TD></TR>
| |
| - | <TR><TD><b>Total Volume</b></TD><TD>50µL</TD></TR>
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - |
| |
| - | <TABLE BORDER>
| |
| - |
| |
| - | <TR><TD><b>Thermocycler Protocol: NEB Phusion</b></TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD>Temp</TD><TD>Time</TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Start</TD><TD>98°C</TD><TD>30 sec</TD><TD>Melt</TD><TD></TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Cycle 1</TD><TD>98°C</TD><TD>5 sec</TD><TD>Melt</TD><TD>35 cycles</TD></TR>
| |
| - | <TR><TD>Cycle 2</TD><TD>40.5°C / 60°C</TD><TD>25 sec</TD><TD>Anneal</TD><TD></TD></TR>
| |
| - | <TR><TD>Cycle 3</TD><TD>72°C</TD><TD>30 sec per kb</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - | <TR><TD> </TD><TD> </TD><TD> </TD><TD> </TD><TD> </TD></TR>
| |
| - | <TR><TD>Finish</TD><TD>72°C</TD><TD>5 min</TD><TD>Extend</TD><TD> </TD></TR>
| |
| - |
| |
| - | <TR><TD>Store</TD><TD>10°C</TD><TD>Forever</TD><TD>Store</TD><TD></TD></TR>
| |
| - |
| |
| - | </TABLE>
| |
| - | <br><br>
| |
| - | <b>Digestion of SPCR 5 and SPCR7</b>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td><td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Purified PCR Product</td><td>16 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td><td>0 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10x FastDigest Buffer</td><td>2 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 1</td><td>1 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 2</td><td>1 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td><td><b>20 ul</b></td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | Incubate at 37°C for 1h shaking<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Purification of Digestion</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 30 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Sunday_25th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Sunday 25<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel of Gradient PCR, Liquid Cultures, Ligation M13 + RFP, Ligation SPCR5, SPCR7, Electrocompetent cells, Gibson Assembly, Transformation (Gibson)and Transformation (Gibson, Ligations.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <b>Gel of Gradient PCR</b><br>
| |
| - | 1%, 100V, 20min<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/b/bd/13%EF%80%A208%EF%80%A225_SPCR2_iS001_iS002.jpg"><br>
| |
| - | <br>
| |
| - | <b>Liquid Cultures</b><br>
| |
| - | NEB Turbo<br>
| |
| - | XL10<br>
| |
| - | <br>
| |
| - | <b>Ligation</b><br>
| |
| - | <br>
| |
| - | <b>Ligation M13 + RFP</b><br>
| |
| - | 0.5ul Vector (M13)<br>
| |
| - | 2.6ul Insert (RFP)<br>
| |
| - | 5.4ul H20<br>
| |
| - | 1.0ul T4 buffer<br>
| |
| - | 0.5ul T4 Ligase<br>
| |
| - | <br>
| |
| - | <b>Ligation SPCR5, SPCR7</b><br>
| |
| - | 1.0ul Vector (SPCR5)<br>
| |
| - | 1.5ul Insert (SPCR7)<br>
| |
| - | 6.0ul H20<br>
| |
| - | 1.0ul T4 buffer<br>
| |
| - | 0.5ul T4 Ligase<br>
| |
| - | <br>
| |
| - | Incubate ~30min at 37 C<br>
| |
| - | <br>
| |
| - | <b>Electrocompetent cells</b><br>
| |
| - | 1) Start Culture<br>
| |
| - | 2) When the cells reach an OD600 of 0.2. <br>
| |
| - | 3) Harvest the cells.<br>
| |
| - | When the cells reach an OD600 of between 0.6 and 0.8 (OD: 0,683)<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | 4) Wash and combine the cells.<br>
| |
| - | Remove the supernatant.<br>
| |
| - | Resuspend the cells in 25 ml of ice cold water<br>
| |
| - | 5) Wash the cells 2 more times.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 50 ml of ice cold water.<br>
| |
| - | Repeat.
| |
| - | 6) Wash and concentrate the cells for electroporation.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 1-2 ml of ice cold water.<br>
| |
| - | We will use 200 ul of washed cells per transformation.<br>
| |
| - | <br>
| |
| - | <b>Gibson Assembly</b><br>
| |
| - | <br>
| |
| - | Amount per Reaction<br>
| |
| - | Positive Control**<br>
| |
| - | <br>
| |
| - | PCR Fragment(s)<br>
| |
| - | + linearized vector<br>
| |
| - | 2-10 μl (0.02–0.5 pmols)*<br>
| |
| - | <br>
| |
| - | Gibson<br>
| |
| - | Assembly Master<br>
| |
| - | Mix (2X)<br>
| |
| - | 10 μl<br>
| |
| - | <br>
| |
| - | Deionized H2O<br>
| |
| - | XX μl<br>
| |
| - | <br>
| |
| - | Total Volume<br>
| |
| - | 20 μl<br>
| |
| - | <br>
| |
| - | Incubate samples in a thermocycler at 50°C for 15 minutes. After incubation, store the samples on ice or at -20°C for subsequent transformation<br>
| |
| - | Note: Extended incubation up to 60 minutes may help to improve assembly efficiency in some cases (for further details see FAQ section).<br>
| |
| - | Transform NEB 5-alpha Competent E. coli cells (provided with the kit) with 2 μl of the assembly reaction, following the transformation protocol.<br>
| |
| - | <br>
| |
| - | <b>Transformation (Gibson)</b><br>
| |
| - | Thaw competent cells on ice.<br>
| |
| - | Add 2 μl of the chilled assembly product to the competent cells. Mix gently by pipetting up and down or by flicking the tube 4–5 times. Do not vortex.<br>
| |
| - | Place the mixture on ice for 30 minutes. Do not mix.<br>
| |
| - | Heat shock at 42°C for 30 seconds. Do not mix.<br>
| |
| - | Transfer tubes to ice for 2 minutes.<br>
| |
| - | Add 950 μl of room-temperature SOC media to the tube.<br>
| |
| - | Incubate the tube at 37°C for 60 minutes. Shake vigorously (250 rpm) or rotate.<br>
| |
| - | Warm selection plates to 37°C.<br>
| |
| - | Spread 100 μl of the cells onto the selection plates. Use Amp plates for positive control sample.<br>
| |
| - | Incubate overnight at 37°C.<br>
| |
| - | <br>
| |
| - | <b>Transformation (Gibson, Ligations)</b><br>
| |
| - | 1) Prepare BD tubes with a pipette filled with LB at the interior of each tube (pipette supplied with the electroporation cuvette)<br>
| |
| - | <br>
| |
| - | 2) Test the purity of the electrocompetent cells.<br>
| |
| - | Add 200 ul of washed cells to a cuvette.<br>
| |
| - | <br>
| |
| - | 3) Mix the cells and DNA in a cuvette.<br>
| |
| - | 200 ul of washed cells with 200 ng of PCR product.<br>
| |
| - | Keep the cuvette on ice until just before the electroporation.<br>
| |
| - | <br>
| |
| - | 4) Preload a pipette with 1 ml of LB.<br>
| |
| - | <br>
| |
| - | 5) Pulse the cuvette with voltage.<br>
| |
| - | Dry the electrodes with a kimwipe prior to loading.<br>
| |
| - | Use the EC2 setting.<br>
| |
| - | <br>
| |
| - | 6) Listen for arcing.<br>
| |
| - | A cracking sound means all the cells are dead.<br>
| |
| - | Note the time constant: 5 is good, 5.8 is great.<br>
| |
| - | <br>
| |
| - | 7) Immediately recover the cells.<br>
| |
| - | Add the 1 ml of preloaded LB and pipet up and down to mix.<br>
| |
| - | Collect 1 ml of cells, some volume is lost in the cuvette.<br>
| |
| - | <br>
| |
| - | 8) Incubate 2 h at 37 °C with shaking.<br>
| |
| - | <br>
| |
| - | 9) Plate 100 ul of recovered cells on selective plates.<br>
| |
| - | Use antibiotic appropriate to the part being integrated.<br>
| |
| - | Let the other 900 ul rest overnight at room temperature.<br>
| |
| - | <br>
| |
| - | 10) Concentrate and plate the remaining cells<br>
| |
| - | Spin down quickly and resuspend in 100 ul LB before plating.<br>
| |
| - | <br>
| |
| - | Transformed cells should be incubated at 37 °C.<br>
| |
| - | Colonies should appear 24-48 h after plating.<br>
| |
| - | <br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Monday_26th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 26<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Picking colonies (Trafo Gibson, BBC SPCR5/7)</b><br>
| |
| - | chosing 5-7 colonies and start liquid cultures
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_27th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 27<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Starting liquid cultures and Miniprep of pS.005 and pS.006.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <b>Starting liquid cultures</b><br>
| |
| - | sSP001, sSP002, sSP010, sSP011, sSP012, sSP020<br>
| |
| - | <br>
| |
| - | <b>Miniprep of pS.005 and pS.006</b><br>
| |
| - | 1) Pellet 2x 9ml of liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250ul of resuspension solution<br>
| |
| - | 4) add 250ul of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350ul of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 ul wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | <b>Colony PCR</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td><td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td><td>0,5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td><td>0,5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template DNA (Miniprep)</td><td>0,5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Quick-Load® Taq 2X Master Mix</td><td>12,5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td><td>10,0 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total volume</b></td><td>25 ul</td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Thermocycler Protocol: Dream Taq Green</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>95°C</td>
| |
| - | <td>30 sec1</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> Cycle 1</td>
| |
| - | <td>95°C</td>
| |
| - | <td>15 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> 35 cycles </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> Cycle 2</td>
| |
| - | <td>46,8°C </td>
| |
| - | <td> 30 sec </td>
| |
| - | <td> Anneal </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> Cycle 3</td>
| |
| - | <td> 68°C </td>
| |
| - | <td> 1 min per kb </td>
| |
| - | <td>Extend</td>
| |
| - | <td>cellule 2</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> Finish</td>
| |
| - | <td> 68°C </td>
| |
| - | <td> 5 min </td>
| |
| - | <td> Extend </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> Store</td>
| |
| - | <td> 10°C </td>
| |
| - | <td>Forever </td>
| |
| - | <td>Store </td>
| |
| - | <td></td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_28th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 28<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel Colony PCR, Liquid Cultures (1:100), Analytical Digest, Gel Ligation/Gibson, Gel Analytical digest, DpnI digest of SPCR5, SPCR6, SPCR7, Gel DpnI digest, PCR purification of DpnI digested SPCR5, SPCR6, SPCR7, Stress test microscope and M13 Test.
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <b>Gel Colony PCR</b><br>
| |
| - | pS005 (C1-C5) - pS006 (C1-C7)<br>
| |
| - | 1% 100V 20 min<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/b/b8/13%EF%80%A208%EF%80%A228_pS005_pS006_Colony_PCR_iS029_iS030.jpg"<br>
| |
| - | <br>
| |
| - | <b>Liquid Cultures (1:100)</b><br>
| |
| - | sSP001, sSP002, sSP010, sSP011, sSP012, sSP020<br>
| |
| - | <br>
| |
| - | <b>Analytical Digest</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td><td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> Plasmid Miniprep </td><td>5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td><td>12 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>c10x FastDigest Buffer</td><td>2ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 1</td><td>0,5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 2</td><td>0,5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td><td> 20,0 ul</td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | Digest for 15 minutes at 37 °C with shaking<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Gel Ligation/Gibson</b><br>
| |
| - | pS005 - pS006 - M13/RFP<br>
| |
| - | 1% 100V 20min<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/7/7d/13%EF%80%A208%EF%80%A228_pS005_pS006_M13%EF%80%A2RFP_Ligation%EF%80%A2Gibson_products.jpg"><br>
| |
| - | <br>
| |
| - | <b>Gel Analytical digest</b><br>
| |
| - | pS005 (C1-C5)-pS006 (C1-C7)<br>
| |
| - | 1% 100V 20min<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/1/1b/13%EF%80%A208%EF%80%A228_pS005_%28C1-C5%29_digested_with_XbaI%EF%80%A2SpeI_pS006_%28C1-C7%29_digested_with_XbaI%EF%80%A2SpeI.jpg"><br>
| |
| - | <br>
| |
| - | <b>DpnI digest of SPCR5, SPCR6, SPCR7</b><br>
| |
| - | add 4ul of DpnI into each tube, mix and incubate for 1h at 37°C<br>
| |
| - | <br>
| |
| - | <b>Gel DpnI digest</b><br>
| |
| - | let each 5ul run on a gel<br>
| |
| - | 1%, 100V 20min<br>
| |
| - | <br>
| |
| - | <b>PCR purification of DpnI digested SPCR5, SPCR6, SPCR7</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 30 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | <b>Stress test microscope</b><br>
| |
| - | Dilute ON cultures of sSP001, sSP002, sSP010, sSP011, sSP012 1:100 and incubate up to an OD of 0.3<br>
| |
| - | Take out 2ml of sSP001, sSP002, sSP010, sSP011<br>
| |
| - | add:<br>
| |
| - | sSP001: 10ug/ml MMC<br>
| |
| - | sSP002: 10ug/ml MMC<br>
| |
| - | sSP010: 20ul sSP012 supernatant<br>
| |
| - | sSP011: 20ul sSP012 supernatant<br>
| |
| - | <br>
| |
| - | incubate for 90 min<br>
| |
| - | <br>
| |
| - | take pictures under the microscope (trans and YFP) of (un-)treated samples<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>M13 Test</b><br>
| |
| - | Liquid cultures of sSP012 and sSP020<br>
| |
| - | 1) 100 μ l of plating bacteria per tube (OD 0.6)<br>
| |
| - | 2) Prepare tenfold serial dilutions (10-6 to 10-9 ) of the bacteriophage stock in LB<br>
| |
| - | 3) Put 10 μ l/ 100 μ l of each dilution to the bacteria<br>
| |
| - | 4) Mix the bacteriophage particles with the bacterial culture by vortexing gently.<br>
| |
| - | 5) Add 40 μ l of X-gal solution (working conc) and IPTG (working conc) solution to each of the tubes<br>
| |
| - | 6) Add 3ml of Agar to each tube and gently vortexing for 3 seconds<br>
| |
| - | 7) Pour the mixture onto plates containing LB medium supplemented with 5 mM MgCl2 and 2x IPTG and Xgal<br>
| |
| - | 8) Swirl the plate gently to ensure an even distribution of bacteria and agar.<br>
| |
| - | 9) Incubate them at 37°C.<br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Friday_30th_August.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Friday 30<sup>th</sup> August</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | M13 test, DpnI digest (SPCR5,6,7), Gel SPCR5,6,7 and PCR purification of DpnI digested SPCR5, SPCR6, SPCR7
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>M13 test</b><br>
| |
| - | dilute ON cultures (NEB turbo, FR-433) 1: 100, grow up to an OD of ~0.6<br>
| |
| - | 1) 100 μ l of plating bacteria per tube (OD 0.6)<br>
| |
| - | 2) Prepare tenfold serial dilutions (10-6 to 10-9 ) of the bacteriophage stock in LB<br>
| |
| - | 3) Put 10 μ l/ 100 μ l of each dilution to the bacteria<br>
| |
| - | 4) Mix the bacteriophage particles with the bacterial culture by vortexing gently.<br>
| |
| - | 5) Add 40 μ l of X-gal solution (working conc) and IPTG (working conc) solution to each of the tubes<br>
| |
| - | 6) Add 3ml of Agar to each tube and gently vortexing for 3 seconds<br>
| |
| - | 7) Pour the mixture onto plates containing LB medium supplemented with 5 mM MgCl2 and 2x IPTG and Xgal<br>
| |
| - | 8) Swirl the plate gently to ensure an even distribution of bacteria and agar.<br>
| |
| - | 9) Incubate them at 37°C.<br>
| |
| - | <br>
| |
| - | <b>DpnI digest (SPCR5,6,7)</b><br>
| |
| - | add 8ul DpnI per tube and digest for 1h at 37°, shaking<br>
| |
| - | <br>
| |
| - | <b>Gel SPCR5,6,7</b><br>
| |
| - | 1%, 100V, 20min<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/7/72/13%EF%80%A208%EF%80%A230_sPCR5_SPCR6_sPCR7_after_DpnI_digest.jpg"height="330"<br>
| |
| - | <br>
| |
| - | <b>PCR purification of DpnI digested SPCR5, SPCR6, SPCR7</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 30 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Tuesday_3rd_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Day Number<sup>suffix</sup> Month</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Place your twit here
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | Place your note here
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_4th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 4<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Starting Liquid culture, PCRs, Gel, DpnI digest, Digestion of SPCR5,7, Purification of Digestion, Ligation of SPCR5,7, Gibson Assembly, Making Electrocompetent Cells, Transformation, Redo SPCR12/13 ,
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Starting Liquid culture</b><br>
| |
| - | NEB turbo, grow up to an OD of 0.6<br>
| |
| - | <br>
| |
| - | <b>PCRs</b><br>
| |
| - | SPCR1, SPCR2, SPCR4, SPCR12, SPCR13<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagant</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td><b>1x (SPCR2)</b></td>
| |
| - | <td><b>11x (SPCR12)</b></td>
| |
| - | <td><b>11x (SPCR13)</b></td>
| |
| - | <td><b>8x (SPCR1)</b></td>
| |
| - | <td><b>8x (SPCR4)</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | <td>447 µl</td>
| |
| - | <td>447 µl</td>
| |
| - | <td>335,25µl</td>
| |
| - | <td>335,25µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | <td>120 µl</td>
| |
| - | <td>120 µl</td>
| |
| - | <td>90 µl</td>
| |
| - | <td>90 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | <td>12 µl</td>
| |
| - | <td>12 µl</td>
| |
| - | <td>9 µl</td>
| |
| - | <td>9 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>4.5 µl</td>
| |
| - | <td>4.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>4.5 µl</td>
| |
| - | <td>4.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid</td>
| |
| - | <td>0.25 µl</td>
| |
| - | <td>3 µl</td>
| |
| - | <td>3 µl</td>
| |
| - | <td>2.25 µl</td>
| |
| - | <td>2.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>4,5 µl</td>
| |
| - | <td>4,5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Total Volume</td>
| |
| - | <td>50 µl</td>
| |
| - | <td>600 µl</td>
| |
| - | <td>600 µl</td>
| |
| - | <td>450 µl</td>
| |
| - | <td>450 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | for SPCR 12/13 gradient, 2,5 min<br>
| |
| - | for SPCR3, SPCR11 51°, 45s<br>
| |
| - | for SPCR 1, SPCR2, 48,8°, 2 min<br>
| |
| - | for SPCR4, 40,8°, 1 min<br>
| |
| - | <br>
| |
| - | <b>Gel</b><br>
| |
| - | 1%, 100V, 20 min<br>
| |
| - | <br>
| |
| - | 1.small gel (SPCR1,2,3,4,11)<br>
| |
| - | 2. big gel (SPCR12)<br>
| |
| - | 3. big Gel (SPCR13)<br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/b/b9/13%EF%80%A209%EF%80%A204_SPCR1%2C2%2C3%2C4%2C11_with_corresponding_primers.jpg"height="320"><br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/1/13/13%EF%80%A209%EF%80%A204_SPCR12_gradient_wrong_programmed_corresponding_primers.jpg"><br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/6/6b/13%EF%80%A209%EF%80%A204_SPCR13_gradient_wrong_programmed_corresponding_primers.jpg"><br>
| |
| - | <br>
| |
| - | <b>DpnI digest</b><br>
| |
| - | SPCR 1: add 10ul DpnI<br>
| |
| - | SPCR4: add 10ul DpnI<br>
| |
| - | SPCR2,3,11: add 1 ul DpnI<br>
| |
| - | <br>
| |
| - | incubate for 1h at 37°<br>
| |
| - | <br>
| |
| - | <b>Digestion of SPCR5,7</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Purified PCR Product</td>
| |
| - | <td>16 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10x FastDigest Buffer</td>
| |
| - | <td>2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>XbaI</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SpeI</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>20.0 µl</td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | Incubate for 1h at 37°, shaking<br>
| |
| - | <br>
| |
| - | <b>Purification of Digestion</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 30 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | <b>Ligation of SPCR5,7</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Vector</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Insert</td>
| |
| - | <td>3 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>4.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | Incubate at room temperature for ~1h<br>
| |
| - | <br>
| |
| - | <b>Gibson Assembly</b><br>
| |
| - | <br>
| |
| - | <b>Amount per Reaction :</b> Positive Control**<br>
| |
| - | <br>
| |
| - | <b>PCR Fragment(s)+ linearized vector :</b> 2-10 μl (0.02–0.5 pmols)*<br>
| |
| - | <br>
| |
| - | <b>Gibson Assembly Master Mix (2X):</b> 10 μl<br>
| |
| - | <br>
| |
| - | <b>Deionized H2O :</b> XX μl<br>
| |
| - | <br>
| |
| - | <b>Total Volume :</b> 20 μl<br>
| |
| - | <br>
| |
| - | Incubate samples in a thermocycler at 50°C for 15 minutes. <br>
| |
| - | Put on Ice<br>
| |
| - | Insert: 2,4 ul<br>
| |
| - | Vector: 0,6 ul<br>
| |
| - | <br>
| |
| - | <b>Making Electrocompetent Cells</b><br>
| |
| - | <br>
| |
| - | 1) Start a liquid culture of cells.
| |
| - | NEB turbo<br>
| |
| - | 2) dilute the cells 100X.<br>
| |
| - | 100 ml LB.<br>
| |
| - | Grow at 30°C for about 90 minutes. <br>
| |
| - | 3) Harvest the cells.<br>
| |
| - | When the cells reach an OD600 of between 0.6 and 0.8<br>
| |
| - | Split the culture into 2x 50 ml falcon tubes, on ice.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | 5) Wash and combine the cells.<br>
| |
| - | Remove the supernatant.<br>
| |
| - | Resuspend the cells in 2x 25 ml of ice cold water.<br>
| |
| - | Combine the volumes in a single 50 ml falcon tube.<br>
| |
| - | 6) Wash the cells 2 more times.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 50 ml of ice cold water.<br>
| |
| - | Repeat.<br>
| |
| - | 7) Wash and concentrate the cells for electroporation.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 1-2 ml of ice cold water.<br>
| |
| - | We will use 200 ul of washed cells per transformation.<br>
| |
| - | <br>
| |
| - | <b>Transformation</b><br>
| |
| - | pS005, pS006, SPCR3 (IDT plasmid) M13mp18<br>
| |
| - | 1) Prepare BD tubes with a pipette filled with LB at the interior of each tube (pipette supplied with the electroporation cuvette)<br>
| |
| - | <br>
| |
| - | 2) Test the purity of the electrocompetent cells.<br>
| |
| - | Add 200 ul of washed cells to a cuvette.<br>
| |
| - | <br>
| |
| - | 3) Mix the cells and DNA in a cuvette.<br>
| |
| - | 200 ul of washed cells with 200 ng of PCR product.<br>
| |
| - | Keep the cuvette on ice until just before the electroporation.<br>
| |
| - | <br>
| |
| - | 4) Preload a pipette with 1 ml of LB.<br>
| |
| - | <br>
| |
| - | 5) Pulse the cuvette with voltage.<br>
| |
| - | Dry the electrodes with a kimwipe prior to loading.<br>
| |
| - | Use the EC2 setting.<br>
| |
| - | <br>
| |
| - | 6) Listen for arcing.<br>
| |
| - | A cracking sound means all the cells are dead.<br>
| |
| - | Note the time constant: 5 is good, 5.8 is great.<br>
| |
| - | <br>
| |
| - | 7) Immediately recover the cells.<br>
| |
| - | Add the 1 ml of preloaded LB and pipet up and down to mix.<br>
| |
| - | Collect 1 ml of cells, some volume is lost in the cuvette.<br>
| |
| - | <br>
| |
| - | 8) Incubate 2 h at 37 °C with shaking.<br>
| |
| - | <br>
| |
| - | 9) Plate 10/200 ul of recovered cells on selective plates.<br>
| |
| - | Use antibiotic appropriate to the part being integrated.<br>
| |
| - | Let the other 900 ul rest overnight at room temperature.<br>
| |
| - | <br>
| |
| - | 10) Concentrate and plate the remaining cells<br>
| |
| - | Spin down quickly and resuspend in 100 ul LB before plating.<br>
| |
| - | <br>
| |
| - | Transformed cells should be incubated at 37 °C.<br>
| |
| - | Colonies should appear 24-48 h after plating.<br>
| |
| - | <br>
| |
| - | <b>Redo SPCR12/13</b>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td><b>11x (SPCR12)</b></td>
| |
| - | <td><b>11x (SPCR13)</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>447 µl</td>
| |
| - | <td>447 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>120 µl</td>
| |
| - | <td>120 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>12 µl</td>
| |
| - | <td>12 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid</td>
| |
| - | <td>3 µl</td>
| |
| - | <td>3 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>6 µl</td>
| |
| - | <td>6 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>600 µl</td>
| |
| - | <td>600 µl</td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | <br>Cycling protocol as usual + gradient + topdown<br>
| |
| - | <br>
| |
| - | <IMG SRC="https://static.igem.org/mediawiki/2013/b/b6/Cycler_protocol_4.9.13.JPG" WIDTH=400>
| |
| - |
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Thursday_5th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 5<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel, Colony PCR, Topdown PCR and gels
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Gel</b><br>
| |
| - | SPCR12, SPCR13<br>
| |
| - | 1%, 100V, 20 min<br>
| |
| - | <br>
| |
| - | Pictures: 13/09/05_SPCR12_corresponding primers<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/7/72/3-09-05_SPCR12_corresponding_primers.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/05_SPCR13_corresponding primers<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/3/32/13-09-05_SPCR13_corresponding_primers.png" width="400"/><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Colony PCR</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)/td>
| |
| - | <td>0.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template DNA (from above)</td>
| |
| - | <td>1.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Quick-Load® Taq 2X Master Mix</td>
| |
| - | <td>12.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>25 ul</td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Thermocycler Protocol: DreamTaq Green PCR MM</b></td>
| |
| - | <td><b> </b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>95°C</td>
| |
| - | <td>1 min </td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>95°C</td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cyle 2</td>
| |
| - | <td>52.6/46.8 °C</td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C </td>
| |
| - | <td>1 min per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72°C</td>
| |
| - | <td>10 min</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | <b>Topdown PCR</b><br>
| |
| - | SPCR 1,4,12,13<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td><b>x1>/b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid</td>
| |
| - | <td>0.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>50 µl</td>
| |
| - | </tr>
| |
| - | </table>
| |
| - | <br>
| |
| - | increases every cycle 1°C, starting from 40°<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Gels</b><br>
| |
| - | 1%, 100V, 20+ Min<br>
| |
| - | <br>
| |
| - | Pictures:<br>
| |
| - | 13/09/05_colony PCR_pS005_C1-C8_BB verification primers<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/6/6b/13-09-05_colony_PCR_pS005_C1-C8_BB_verification_primers.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/05_colony PCR_pS005_C9-C16_BB verification primers<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/5/50/13-09-05_colony_PCR_pS005_C9-C16_BB_verification_primers.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/05_colony PCR_pS006_C1-C8_BB verification primers<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/b/be/3-09-05_colony_PCR_pS006_C1-C8_BB_verification_primers.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/05_colony PCR_pS006_C9-C16_BB verification primers<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/0/05/3-09-05_colony_PCR_pS006_C9-C16_BB_verification_primers.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/05_top down PCR_SPCR1,4,12,13<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/1/19/13-09-05_top_down_PCR_SPCR1%2C4%2C12%2C13.png" width="400"/><br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Friday_6th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Friday 6<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Place your twit here
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | Digestions: linearized pSB1C3, linearized pSB1A3, SPCR2, SPCR3, SPCR11<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Purified PCR Product</td>
| |
| - | <td>16 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2OH2O</td>
| |
| - | <td>0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10x FastDigest Buffer</td>
| |
| - | <td>2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 1</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>cFastDigest Enzyme 2</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>4 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR5, pSB1C3: XbaI/SpeI<br>
| |
| - | SPCR11, pSB1A3, pSB1C3: EcoRI/PstI<br>
| |
| - | SPCR13, pSB1A3, pSB1C3: EcoRI/PstI<br>
| |
| - | SPCR2, pSB1A3, pSB1C3: EcoRI/PstI<br>
| |
| - | <br>
| |
| - | 1h at 37° shaking<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Saturday_7th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Saturday 7<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Ligation, Making Electrocompetent Cells, Gibson Assembly, Transformation, Liquid culture of E1010
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Ligation</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Vector</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Insert</td>
| |
| - | <td>3 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>4.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR5, pSB1C3<br>
| |
| - | SPCR11, pSB1A3, pSB1C3<br>
| |
| - | SPCR13, pSB1A3, pSB1C3<br>
| |
| - | SPCR2, pSB1A3, pSB1C3<br>
| |
| - | <br>
| |
| - | Incubate at room temperature for 10 minutes.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Making Electrocompetent Cells</b><br>
| |
| - | 1) Start a liquid culture of cells.<br>
| |
| - | NEB turbo<br>
| |
| - | 2) dilute the cells 100X.<br>
| |
| - | 100 ml LB.<br>
| |
| - | Grow at 30°C for about 90 minutes. <br>
| |
| - | 3) Harvest the cells.<br>
| |
| - | When the cells reach an OD600 of between 0.6 and 0.8<br>
| |
| - | Split the culture into 2x 50 ml falcon tubes, on ice.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | 5) Wash and combine the cells.<br>
| |
| - | Remove the supernatant.<br>
| |
| - | Resuspend the cells in 2x 25 ml of ice cold water.<br>
| |
| - | Combine the volumes in a single 50 ml falcon tube.<br>
| |
| - | 6) Wash the cells 2 more times.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 50 ml of ice cold water.<br>
| |
| - | Repeat.<br>
| |
| - | 7) Wash and concentrate the cells for electroporation.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 1-2 ml of ice cold water.<br>
| |
| - | We will use 200 ul of washed cells per transformation.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Gibson Assembly</b><br>
| |
| - | <br>
| |
| - | Amount per Reaction<br>
| |
| - | Positive Control**<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | PCR Fragment(s)<br>
| |
| - | + linearized vector<br>
| |
| - | 2-10 μl (0.02–0.5 pmols)*<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | Gibson<br>
| |
| - | Assembly Master<br>
| |
| - | Mix (2X)<br>
| |
| - | 10 μl<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | Deionized H2O<br>
| |
| - | XX μl
| |
| - | <br>
| |
| - | <br>
| |
| - | Total Volume<br>
| |
| - | 20 μl<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <br>
| |
| - | Incubate samples in a thermocycler at 50°C for 15 minutes. <br>
| |
| - | Put on Ice<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Transformation</b>
| |
| - | pS002 (Chl), pS002 (Amp), pS003 (Amp), pS004 (Chl), pS004 (Amp), pS005 (Chl), pS006-7 (Chl), pS007 (Chl), pS008 (Amp), pS009 (Chl), pS012 (Amp), pS013 (Chl), pS013 (Amp) <br>
| |
| - | <br>
| |
| - | 1) Prepare BD tubes with a pipette filled with LB at the interior of each tube (pipette supplied with the electroporation cuvette)<br>
| |
| - | <br>
| |
| - | 2) Test the purity of the electrocompetent cells.<br>
| |
| - | Add 200 ul of washed cells to a cuvette.<br>
| |
| - | <br>
| |
| - | 3) Mix the cells and DNA in a cuvette.<br>
| |
| - | 200 ul of washed cells with 200 ng of PCR product.<br>
| |
| - | Keep the cuvette on ice until just before the electroporation.<br>
| |
| - | <br>
| |
| - | 4) Preload a pipette with 1 ml of LB.<br>
| |
| - | <br>
| |
| - | 5) Pulse the cuvette with voltage.<br>
| |
| - | Dry the electrodes with a kimwipe prior to loading.<br>
| |
| - | Use the EC2 setting.<br>
| |
| - | <br>
| |
| - | 6) Listen for arcing.<br>
| |
| - | A cracking sound means all the cells are dead.<br>
| |
| - | Note the time constant: 5 is good, 5.8 is great.<br>
| |
| - | <br>
| |
| - | 7) Immediately recover the cells.<br>
| |
| - | Add the 1 ml of preloaded LB and pipet up and down to mix.<br>
| |
| - | Collect 1 ml of cells, some volume is lost in the cuvette.<br>
| |
| - | <br>
| |
| - | 8) Incubate 1/2 h at 37 °C with shaking.<br>
| |
| - | <br>
| |
| - | 9) Plate 10/200 ul of recovered cells on selective plates.<br>
| |
| - | Use antibiotic appropriate to the part being integrated.<br>
| |
| - | Let the other 900 ul rest overnight at room temperature.<br>
| |
| - | <br>
| |
| - | 10) Concentrate and plate the remaining cells<br>
| |
| - | Spin down quickly and resuspend in 100 ul LB before plating.<br>
| |
| - | <br>
| |
| - | Transformed cells should be incubated at 37 °C.<br>
| |
| - | Colonies should appear 24-48 h after plating.<br>
| |
| - | <br>
| |
| - | <b>Liquid culture of E1010</b><br>
| |
| - |
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Sunday_8th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Sunday 8<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Replating of transformation and Miniprep of E1010
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <b>Replating of Transformation</b><br>
| |
| - | <br>
| |
| - | <b>Miniprep of E1010</b><br>
| |
| - | 1) Pellet liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250ul of resuspension olution<br>
| |
| - | 4) add 250ul of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350ul of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 ul wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Monday_16th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 16<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Result Cloning, Protocol: E. coli Colony PCR, Extraction of DNA, PCR Reaction and Gels
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <b>Result Cloning:</b><br>
| |
| - | Colonies?<br>
| |
| - | pS002 (Chl): no<br>
| |
| - | pS002 (Amp): yes<br>
| |
| - | pS003 (Amp):yes<br>
| |
| - | pS004 (Chl): no<br>
| |
| - | pS004 (Amp): yes<br>
| |
| - | pS005 (Chl): yes<br>
| |
| - | pS006-7 (Chl): yes<br>
| |
| - | pS006 (Chl): no<br>
| |
| - | pS007 (Chl): yes<br>
| |
| - | pS008 (Amp): yes<br>
| |
| - | pS009 (Chl): yes<br>
| |
| - | pS012 (Amp): yes<br>
| |
| - | pS013 (Chl): no<br>
| |
| - | pS013 (Amp): yes<br>
| |
| - | <br>
| |
| - | <b>Protocol: E. coli Colony PCR</b><br>
| |
| - | Using the Dream Taq Master Mix<br>
| |
| - | <br>
| |
| - | <b>Extraction of DNA</b><br>
| |
| - | <br>
| |
| - | 1) Pick a single colony into 50 ul of H20.<br>
| |
| - | <br>
| |
| - | 2) Boil for 5 minutes.<br>
| |
| - |
| |
| - | <br>
| |
| - | <b>PCR Reaction (pS002 (Chl-Lig), pS005 (Chl-G), pS006-7 (Chl-Lig), pS007 (Chl-G), pS008 (Amp-G), pS009 (Chl-G))</b><br>
| |
| - | <br>
| |
| - | Keep all the reagents at 4 °C while preparing the mixture.<br>
| |
| - | Pre-heat the thermocycler to 95 °C and transfer your reaction directly from 4 °C.<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template DNA (from above)</td>
| |
| - | <td>1.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Quick-Load® Taq 2X Master Mix</td>
| |
| - | <td>12.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>10 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>25 ul</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Thermocycler Protocol: NEB Quick-Load</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>95°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>95°C</td>
| |
| - | <td>15 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td>45.8 °C</td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>1 min per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>15 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Gels</b><br>
| |
| - | 100V, 25-30 min, 1%<br>
| |
| - | <br>
| |
| - | Pictures: <br>
| |
| - | 13/09/16_colony PCR_ps007.BMP<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/5/50/13-09-16_colony_PCR_ps007.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/16_colony PCR_pS006-7.BMP<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/8/8d/13-09-16_colony_PCR_pS006-7.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/16_colony PCR_ps005.BMP<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/a/a6/13-09-16_colony_PCR_ps005.png" width="400"/><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | Result: didn’t work<br>
| |
| - | <br>
| |
| - | </table>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_17th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 17<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | PCR Reaction (pS003 (Amp-G), pS004 (Amp-Lig), pS012 (Amp-G), pS013 (Chl-Lig))
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>PCR Reaction (pS003 (Amp-G), pS004 (Amp-Lig), pS012 (Amp-G), pS013 (Chl-Lig))</b><br>
| |
| - | <br>
| |
| - | Keep all the reagents at 4 °C while preparing the mixture.<br>
| |
| - | Pre-heat the thermocycler to 95 °C and transfer your reaction directly from 4 °C.<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template DNA (from above)</td>
| |
| - | <td>1.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Quick-Load® Taq 2X Master Mix</td>
| |
| - | <td>12.5 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>10 ul</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>25 ul</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Thermocycler Protocol: NEB Quick-Load</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>95°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>95°C</td>
| |
| - | <td>15 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td>45.8 °C</td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>1 min per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>15 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Gels</b><br>
| |
| - | 100V, 30 min, 1%<br>
| |
| - | <br>
| |
| - | <b>Pictures:</b>
| |
| - | 13/09/17_colony PCR_pS009.JPG<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/b/b5/13-09-17_colony_PCR_pS013.JPG" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/17_colony PCR_pS008_pS002.jpg<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/c/c0/13-09-17_colony_PCR_pS008_pS002.jpg" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/17_colony PCR_pS003.JPG<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/f/fb/13-09-17_colony_PCR_pS003.JPG" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/17_colony PCR_pS004.JPG<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/a/a4/13-09-17_colony_PCR_pS004.JPG" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/17_colony PCR_pS012.JPG<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/1/19/13-09-17_colony_PCR_pS012.JPG" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/17_colony PCR_pS013.JPG<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/f/f7/13-09-17_colony_PCR_pS013.2.JPG" width="400"/><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Result: </b><br>
| |
| - | pS003: row 3,5 might have worked -> analytical digest<br>
| |
| - | pS004: all might have worked -> analytical digest<br>
| |
| - | pS013: all might have worked -> analytical digest<br>
| |
| - | pS012: row 3,4,5 might have workes -> analytical digest<br>
| |
| - | <br>
| |
| - | <b>Sequencing</b><br>
| |
| - | Bringing primers/plasmids away for sequencin<br>
| |
| - | Bacbbone, SPCR2 with iS002, iS032, iS028, iS029, iS030<br>
| |
| - | <br>
| |
| - |
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_18th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 16<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Ligations
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - |
| |
| - | <b>Ligation</b><br>
| |
| - | <br>
| |
| - | SPCR2 - Chl <br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR2</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Chl</td>
| |
| - | <td>2,95 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>4.55 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1.0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR2 - Amp<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR2</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Amp</td>
| |
| - | <td>3.4 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>4.1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1.0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR3 - Chl<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR3</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Amp</td>
| |
| - | <td>1.79 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>5.71 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1.0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR3 - Amp7
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Amp</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR 3</td>
| |
| - | <td>1.56 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>5.94 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1.0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR5 - Chl<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR 5</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Chl</td>
| |
| - | <td>4.55 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>3.45 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1.0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR11 - Chl<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Chl</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR11</td>
| |
| - | <td>1.3 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>6.2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1.0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR2 - Amp<br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Amp</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR11</td>
| |
| - | <td>1.13 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>6.37 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1.0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzyme</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | at 16° for 1h<br>
| |
| - | <br>
| |
| - | <b>Transformation</b><br>
| |
| - | 1) Thaw competent cells on ice (Gibson Kit competent cells)<br>
| |
| - | 2) Place 20 ul of cells in a pre-chilled Eppendorf tube.<br>
| |
| - | 3) Add 2.5 ul of plasmid (from Biobrick stock)<br>
| |
| - | 4) Mix gently by flicking the tube.<br>
| |
| - | 5) Chill on ice for 10 minutes.<br>
| |
| - | 4) Heat shock at 42 °C for 30 seconds <br>
| |
| - | 5) Return to ice for 2 minutes.<br>
| |
| - | 6) Add 200 ul LB medium and recover the cells by shaking at 37 °C.<br>
| |
| - | Ampicillin: 15-30 minutes<br>
| |
| - | Chloramphenicol: 60-120 minutes<br>
| |
| - | 7) Plate out the cells on selective LB (10ul)<br>
| |
| - | 8. Incubate at 37 °C. Transformants should appear within 12 hrs.<br>
| |
| - | <br>
| |
| - | <b>Gel of Ligation products</b><br>
| |
| - | 1%, 100V, 40 min<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Sunday_22nd_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Sunday 22<sup>nd</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | PCR and Gels
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>PCR</b><br>
| |
| - | M13 backbone<br>
| |
| - | <br>
| |
| - | SPCR16,17<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td><b>x1</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid</td>
| |
| - | <td>0.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>50 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | Protocol see fotos<br>
| |
| - | <br>
| |
| - | <b>Gel</b>
| |
| - | 100V, 1%, 1,5h<br>
| |
| - | <br>
| |
| - |
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Monday_23rd_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 23<sup>rd</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gels and PCR
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <b>Gel</b><br>
| |
| - | 100V, 1%, 1,5h<br>
| |
| - | <br>
| |
| - | Picture: 13/09/23_SPCR16_17_corresponding primers - PCRs didn't worked<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/0/0e/13-09-23_SPCR16_17_corresponding_primers.JPG" width="400"/><br>
| |
| - | <br>
| |
| - | <b>PCR</b><br>
| |
| - | SPCR 16 (normal phusion at 48°C)<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td><b>x1</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid</td>
| |
| - | <td>0.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>50 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Thermocycler Protocol: NEB Phusion</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>98°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>98°C</td>
| |
| - | <td>5 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td>72°C</td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>30 sec per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>5 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br><br>
| |
| - | <br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_24th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 24<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Overlap PCR, PCR of Overlap, Digestion, Gel extraction, Gels, PCR Purification, PCR (SPCR2, SPCR3, SPCR5, SPCR6, SPCR7, SPCR8, SPCR9, SPCR10, SPCR11, linearize pSB1C3) and liquid culture
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Overlap PCR</b><br>
| |
| - | SPCR5-SPCR2<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td><b>x1</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid(10 uM)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid (10 uM)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>50 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/8/8b/PB_labbooksensor01.JPG" width="300"><br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/6/6b/PB_labbooksensor02.JPG" width="300"><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>PCR of Overlap</b><br>
| |
| - | <br>
| |
| - | <b>Digestion</b><br>
| |
| - | M13 (EcoRI, PstI), pSB1C3 (EcoRI, PstI), psB1C3 (XbaI, SpeI)<br>
| |
| - | <br>
| |
| - |
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Purified Plasmid</td>
| |
| - | <td>20 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>63 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10x FastDigest Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 1</td>
| |
| - | <td>2.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 2</td>
| |
| - | <td>2.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastAP Phosphatase</td>
| |
| - | <td>2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>100 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | SPCR2 (EcoRI, PstI), SPCR5 (XbaI, SpeI)<br>
| |
| - | <br>
| |
| - |
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Purified PCR Product</td>
| |
| - | <td>16 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10x FastDigest Buffer</td>
| |
| - | <td>2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 1</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 2</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>20 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <b>Gel</b><br>
| |
| - | pSB1C3<br>
| |
| - | 1%, 100V, 1h<br>
| |
| - | Picture: 13/09/24_pSB1C3 digest_EcoRI/PstI_XbaI/SpeI - digest worked<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/e/ec/13-09-24_pSB1C3_digest_EcoRI-PstI_XbaI-SpeI.JPG" width="400"/><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Gel extraction</b><br>
| |
| - | 1. Excise the DNA fragment from the agarose gel with a clean, sharp scalpel. Minimize the size of the gel slice by removing extra agarose.<br>
| |
| - | 2. Weigh the gel slice in a colorless tube. Add 3 volumes of Buffer QG to 1 volume of gel (100 mg ~ 100 μl). To help dissolve gel, mix by vortexing the tube every 2–3 min during the incubation.<br>
| |
| - | 3. After the gel slice has dissolved completely, check that the color of the mixture is yellow (similar to Buffer QG without dissolved agarose).<br>
| |
| - | 4. Add 1 gel volume of isopropanol to the sample and mix (actually only needed for very small products or very big products)
| |
| - | 5. To bind DNA, apply the sample to the QIAquick column, and centrifuge for 1 min.<br>
| |
| - | 6. Discard flow-through and place QIAquick column back in the same collection tube.<br>
| |
| - | 7. To wash, add 0.75 ml of Buffer PE to QIAquick column and centrifuge for 1 min.<br>
| |
| - | 8. Discard the flow-through and centrifuge the QIAquick column for an additional 1 min at 17,900 x g (13,000 rpm).<br>
| |
| - | 9. Place QIAquick column into a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | 10. To elute DNA, add 30 μl elution buffer to the center of the QIAquick membrane, let the column stand for 1 min, and then centrifuge for 1 min.<br>
| |
| - | <br>
| |
| - | <b>Gel</b><br>
| |
| - | PCR Overlap<br>
| |
| - | 1%, 100V, 1h<br>
| |
| - | Picture: 13/09/24_Overlap PCR PCR SCPR5_SPCR2 - PCR didn't work<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/e/e8/13-09-24_Overlap_PCR_PCR_SCPR5_SPCR2.png" width="400"/><br>
| |
| - | <br>
| |
| - | <b>PCR Purification (M13 (EcoRI, PstI), SPCR2 (EcoRI, PstI), SPCR5 (XbaI, SpeI))</b><br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 50 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - | <br>
| |
| - | <b>PCR (SPCR2, SPCR3, SPCR5, SPCR6, SPCR7, SPCR8, SPCR9, SPCR10, SPCR11, linearize pSB1C3)</b><br>
| |
| - | each 8x<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td></td>
| |
| - | <td><b>1x</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid</td>
| |
| - | <td>0.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>50 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <table border="1"><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <tr>
| |
| - | <td><b>Thermocycler Protocol: Fermentas Phusion</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>98°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>98°C</td>
| |
| - | <td>5 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td> </td>
| |
| - | <td>25 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>30 sec per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>5 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <b>Liquid culture</b><br>
| |
| - | NEB, sSP004, Fr-433<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_25th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 25<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel of PCR, PCR (SPCR5,6) and Miniprep Cas9, M13mp18
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Gel of PCR</b><br>
| |
| - | 1%, 100V, 1h<br>
| |
| - | <br>
| |
| - | Picture: 13/09/25_SPCR2-11 - SPCR2: worked, SPCR3: worked, SPCR5: didn't work, SPCR6: didn't work, SPCR7: didn't work, SPCR8: didn't work, SPCR9: didn't work, SPCR10: didn't work, SCPR11: worked <br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/c/ca/13-09-25_SPCR2-10.png" width="400"/><br>
| |
| - | <br>
| |
| - | <b>PCR (SPCR5,6)</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td><b>x1</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid)</td>
| |
| - | <td>0.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>50 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <td><b>Thermocycler Protocol: Fermentas Phusion</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>98°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>98°C</td>
| |
| - | <td>5 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td> </td>
| |
| - | <td>25 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>30 sec per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>5 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <b>Miniprep Cas9, M13mp18</b><br>
| |
| - | 1) Pellet liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250ul of resuspension olution<br>
| |
| - | 4) add 250ul of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350ul of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 ul wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Thursday_26th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 26<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel PCR 5,6, Digestion, PCR (SPCR7-10) and PCR purification
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Gel PCR 5,6</b>
| |
| - | 1%, 100V, 1h<br>
| |
| - | <br>
| |
| - | Picture: 13/09/26_SPCR5_6 - PCR didn't work<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/b/b2/13-09-26_SPCR5_6.png"><br>
| |
| - | <br>
| |
| - | <b>Digestions: SPCR2 (EcoRI, PstI), SPCR3 (EcoRI, PstI), SPCR4 (EcoRI, PstI), SPCR11 (EcoRI, PstI), lin pSB1C3 (EcoRI, PstI), lin pSB1A3 (EcoRI, PstI), SPCR5 (XbaI, SpeI), SPCR7 (XbaI, SpeI), lin pSB1C3 (XbaI, SpeI), in pSB1A3 (XbaI, SpeI)</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Purified PCR Product</td>
| |
| - | <td>16 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>0 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10x FastDigest Buffer</td>
| |
| - | <td>2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 1</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>FastDigest Enzyme 2</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>20 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <b>PCR (SPCR7-10)</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td><b>x1</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid)</td>
| |
| - | <td>0.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>50 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <td><b>Thermocycler Protocol: Fermentas Phusion</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>98°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>98°C</td>
| |
| - | <td>5 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td> </td>
| |
| - | <td>25 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>30 sec per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>5 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>PCR Purification: (SPCR2 (EcoRI, PstI), SPCR3 (EcoRI, PstI), SPCR4 (EcoRI, PstI), SPCR11 (EcoRI, PstI), lin pSB1C3 (EcoRI, PstI), lin pSB1A3 (EcoRI, PstI), SPCR5 (XbaI, SpeI), SPCR7 (XbaI, SpeI), lin pSB1C3 (XbaI, SpeI), in pSB1A3 (XbaI, SpeI)</b><br>
| |
| - | <br>
| |
| - | Add 5 volumes of Buffer PB to 1 volume of the PCR sample and mix.<br>
| |
| - | To bind DNA, apply the sample to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through. Place the QIAquick column back into the same tube<br>
| |
| - | To wash, add 0.75 ml Buffer PE to the QIAquick column and centrifuge for 30–60 s.<br>
| |
| - | Discard flow-through and place the QIAquick column back in the same tube.<br>
| |
| - | Centrifuge the column for an additional 1 min.<br>
| |
| - | Place QIAquick column in a clean 1.5 ml microcentrifuge tube.<br>
| |
| - | To elute DNA, add 50 μl Buffer EB to the center of the QIAquick membrane and centrifuge the column for 1 min.<br>
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Friday_27th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Friday 27<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Gel SPCR7-10, NEB liquid culture, Ligation, Electrocompetent cells and transformation
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Gel SPCR7-10</b><br>
| |
| - | 1%, 100V, 1h<br>
| |
| - | <br>
| |
| - | Picture: 13/09/27_SPCR7_8_9_10 - PCRs worked<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/9/91/13-09-27_SPCR7_8_9_10.png" width="400"/><br>
| |
| - | <br>
| |
| - | <b>NEB liquid culture</b><br>
| |
| - | 1:1000 of ON culture<br>
| |
| - | <br>
| |
| - | <b>Ligation</b><br>
| |
| - | <br>
| |
| - | pS006<br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR5</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR7</td>
| |
| - | <td>0,28 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>7.22 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS006’
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR5</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>lin pSB1C3 (XbaI/SpeI)</td>
| |
| - | <td>0,47 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>7.03 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS006*
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR5</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>lin pSB1A3 (XbaI/SpeI)</td>
| |
| - | <td>0,67 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>6.83 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS013
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR4</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR11</td>
| |
| - | <td>0,24 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>7.26 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS013'
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>lin pSB1C3 (EcoRI, SpeI)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR11</td>
| |
| - | <td>0,28 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>7.22 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS013*
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>lin pSB1A3 (EcoRI, PstI))</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR11</td>
| |
| - | <td>0,3 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>7.2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS004
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR4</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR3</td>
| |
| - | <td>0,2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>7.3 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS004'
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>lin pSB1C3 (EcoRI, PstI)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR3</td>
| |
| - | <td>0,3 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>7.2 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS004*
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>lin pSB1A3 (EcoRI, PstI)</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR3</td>
| |
| - | <td>0,27 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>7.23 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS002'
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR2</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>lin pSB1C3 (EcoRI, PstI)</td>
| |
| - | <td>0,8 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>6.7 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | pS002*
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>SPCR2</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>lin pSB1A3 (EcoRI, PstI)</td>
| |
| - | <td>0,6 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>H2O</td>
| |
| - | <td>6.9 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Buffer</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Fermentas T4 Ligase Enzime</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | 45min at 22°, 15 min at 16°<br>
| |
| - | <br>
| |
| - | <b>Electrocompetent cells</b><br>
| |
| - | 1) Start Culture<br>
| |
| - | 2) When the cells reach an OD600 of 0.2. <br>
| |
| - | 3) Harvest the cells.<br>
| |
| - | When the cells reach an OD600 of between 0.6 and 0.8 (OD: 0,683)<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | 4) Wash and combine the cells.<br>
| |
| - | Remove the supernatant.<br>
| |
| - | Resuspend the cells in 25 ml of ice cold water<br>
| |
| - | 5) Wash the cells 2 more times.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 50 ml of ice cold water.<br>
| |
| - | Repeat.<br>
| |
| - | 6) Wash and concentrate the cells for electroporation.<br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.<br>
| |
| - | Resuspend in 1-2 ml of ice cold water.<br>
| |
| - | We will use 200 ul of washed cells per transformation.<br>
| |
| - | <br>
| |
| - | <b>Transformation</b><br>
| |
| - | pS006, pS006’, pS006*, pS013, pS013’, pS013*, pS004, pS004’, pS004*, pS002’, pS002*<br>
| |
| - | <br>
| |
| - | 1) Prepare BD tubes with a pipette filled with LB at the interior of each tube (pipette supplied with the electroporation cuvette)<br>
| |
| - | <br>
| |
| - | 2) Test the purity of the electrocompetent cells.<br>
| |
| - | Add 200 ul of washed cells to a cuvette.<br>
| |
| - | <br>
| |
| - | 3) Mix the cells and DNA in a cuvette.<br>
| |
| - | 200 ul of washed cells with 200 ng of PCR product.<br>
| |
| - | Keep the cuvette on ice until just before the electroporation.<br>
| |
| - | <br>
| |
| - | 4) Preload a pipette with 1 ml of LB.<br>
| |
| - | <br>
| |
| - | 5) Pulse the cuvette with voltage.<br>
| |
| - | Dry the electrodes with a kimwipe prior to loading.<br>
| |
| - | Use the EC2 setting.<br>
| |
| - | <br>
| |
| - | 6) Listen for arcing.<br>
| |
| - | A cracking sound means all the cells are dead.<br>
| |
| - | Note the time constant: 5 is good, 5.8 is great.<br>
| |
| - | <br>
| |
| - | 7) Immediately recover the cells.<br>
| |
| - | Add the 1 ml of preloaded LB and pipet up and down to mix.<br>
| |
| - | Collect 1 ml of cells, some volume is lost in the cuvette.<br>
| |
| - | <br>
| |
| - | 8) Incubate 1/2 h at 37 °C with shaking.<br>
| |
| - | <br>
| |
| - | 9) Plate 10/200 ul of recovered cells on selective plates.<br>
| |
| - | Use antibiotic appropriate to the part being integrated.<br>
| |
| - | Let the other 900 ul rest overnight at room temperature.<br>
| |
| - | <br>
| |
| - | 10) Concentrate and plate the remaining cells<br>
| |
| - | Spin down quickly and resuspend in 100 ul LB before plating.<br>
| |
| - | <br>
| |
| - | Transformed cells should be incubated at 37 °C.<br>
| |
| - | Colonies should appear 24-48 h after plating.<br>
| |
| - | <br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Saturday_28th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Saturday 28<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Extraction of Genomic DNA, PCR Reaction and Restreak plates
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Protocol: E. coli Colony PCR (pS006’, pS006*, pS013, pS004, pS004*, pS002*)</b><br>
| |
| - | <br>
| |
| - | <b>Extraction of Genomic DNA</b><br>
| |
| - | <br>
| |
| - | 1) Pick a single colony into 50 ul of H20.<br>
| |
| - | Fresh colonies (grown that day) work best, but they can also come from 4 C.<br>
| |
| - | Pipet 2ul onto plates to have C1-C8<br>
| |
| - | Pipet 2 ul into 5ml Media with antibiotics to make liquid cultures<br>
| |
| - | <br>
| |
| - | 2) Boil for 5 minutes.<br>
| |
| - | 1.5 ul of this can be used directly for PCR.<br>
| |
| - | Best if used directly, but can also be stored at 4 C for a few days.<br>
| |
| - | <br>
| |
| - | <b>PCR Reaction</b><br>
| |
| - | <br>
| |
| - | Keep all the reagents at 4 °C while preparing the mixture.<br>
| |
| - | Pre-heat the thermocycler to 95 °C and transfer your reaction directly from 4 °C.<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | <td><b>9x Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | <td>4.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | <td>4.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template DNA (from above)</td>
| |
| - | <td>1.5 µl</td>
| |
| - | <td>13.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Quick-Load® Taq 2X Master Mix</td>
| |
| - | <td>12.5 µl</td>
| |
| - | <td>112.5 µl9x Volume</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>10 µl</td>
| |
| - | <td>90 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>25 µl</td>
| |
| - | <td>125 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <td><b>Thermocycler Protocol: Green Dream Taq</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>95°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>95°C</td>
| |
| - | <td>15 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td>46.8°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>1 min per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>10 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <b>Restreak plates</b><br>
| |
| - | Some of the plates were too full grown -> Rstreak for single colonies<br>
| |
| - |
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Sunday_29th_September.html"</div></html>
| |
| - | <html><div id="detect_Monday_30th_September.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 30<sup>th</sup> September</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Extraction of Genomic DNA, PCR reaction, Gels, Miniprep, PCR: SPCR5, SPCR6 and Liquid culture of pS004’ and pS013’
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Protocol: E. coli Colony PCR (pS006, pS013’,pS013*, pS004’, pS002’)</b><br>
| |
| - | <br>
| |
| - | <b>Extraction of Genomic DNA</b><br>
| |
| - | <br>
| |
| - | 1) Pick a single colony into 50 ul of H20.<br>
| |
| - | Fresh colonies (grown that day) work best, but they can also come from 4 C.<br>
| |
| - | Pipet 2ul onto plates to have C1-C8<br>
| |
| - | <br>
| |
| - | 2) Boil for 5 minutes.<br>
| |
| - | 1.5 ul of this can be used directly for PCR.<br>
| |
| - | Best if used directly, but can also be stored at 4 C for a few days.<br>
| |
| - | <br>
| |
| - | <b>PCR Reaction</b><br>
| |
| - | <br>
| |
| - | Keep all the reagents at 4 °C while preparing the mixture.<br>
| |
| - | Pre-heat the thermocycler to 95 °C and transfer your reaction directly from 4 °C.<br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | <td><b>9x Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | <td>4.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | <td>4.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template DNA (from above)</td>
| |
| - | <td>1.5 µl</td>
| |
| - | <td>13.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Quick-Load® Taq 2X Master Mix</td>
| |
| - | <td>12.5 µl</td>
| |
| - | <td>112.5 µl9x Volume</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>10 µl</td>
| |
| - | <td>90 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>25 µl</td>
| |
| - | <td>125 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <td><b>Thermocycler Protocol: Green Dream Taq</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>95°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>95°C</td>
| |
| - | <td>15 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td>46.8°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>1 min per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>10 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <b>Gels</b><br>
| |
| - | 1%, 100V, 45 min<br>
| |
| - | <br>
| |
| - |
| |
| - | Pictures + Results<br>
| |
| - | 13/09/30_colony pcr_pS004_pS013 - 1-8: pS004 (gRNA - Amp), 9-16: pS013 (crRNA - Amp) - seems to have worked beside pS013 C7<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/c/c5/13-09-30_colony_pcr_pS004_pS013.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/30_colony PCR_pS004*_pS002* - 1-8: pS004* (gRNA - Amp), 9-16: pS002 (reporter - Amp) - pS004* seems to have worked (C1, C2, C3, C6)<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/2/20/3-09-30_colony_PCR_pS004%2A_pS002%2A.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/30_colony PCR_pS006'_pS006* - 1-8: pS006' (Cas9 - Chl), 9-16: pS006* (Cas9 - Amp) - didn’t work<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/4/44/13-09-30_colony_PCR_pS006%27_pS006%2A.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/30_Colony PCR_pS013'_pS013* - 1-8: pS013' (crRNA - Chl), 9-16: pS013* (crRNA - Amp) - Seems to have worked beside 13’ C7, C8<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/c/ca/13-09-30_Colony_PCR_pS013%27_pS013%2A.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/30_colony PCR_pS004'_pS002' - 1-8: pS004' (gRNA - Chl), 9-16: pS002' (reporter - Chl) - pS004' seems to have worked beside C6<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/9/9f/13-09-30_colony_PCR_pS004%27_pS002%27.png" width="400"/><br>
| |
| - | <br>
| |
| - | 13/09/30_Colony PCR_pS006 - didn’t work<br>
| |
| - | <img src="https://static.igem.org/mediawiki/2013/b/bf/13-09-30_Colony_PCR_pS006.png" width="400"/><br>
| |
| - | <br>
| |
| - | other gel images that proof that the reporter as well as the Cas9 construct worked will follow soon!
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Miniprep</b><br>
| |
| - | pS013, pS004<br>
| |
| - | 1) Pellet liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250ul of resuspension olution<br>
| |
| - | 4) add 250ul of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350ul of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 ul wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <br>
| |
| - | <b>PCR: SPCR5, SPCR6 (gradient + touch down 55-75, -1°/cycle)</b><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <tr>
| |
| - | <td><b>Reagent</b></td>
| |
| - | <td><b>Volume</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td></td>
| |
| - | <td><b>11x</b></td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Nuclease-free water</td>
| |
| - | <td>37.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>5x Phusion HF Buffer</td>
| |
| - | <td>10 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>10 mM dNTPs</td>
| |
| - | <td>1 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Forward Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Reverse Primer (10 uM)</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Template Plasmid)</td>
| |
| - | <td>0.25 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Phusion DNA Polymerase</td>
| |
| - | <td>0.5 µl</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td><b>Total Volume</b></td>
| |
| - | <td>50 µl</td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <table border="1">
| |
| - | <td><b>Thermocycler Protocol: Fermentas Phusion</b></td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td>Temp</td>
| |
| - | <td>Time</td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Start</td>
| |
| - | <td>98°C </td>
| |
| - | <td>30 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 1</td>
| |
| - | <td>98°C</td>
| |
| - | <td>5 sec</td>
| |
| - | <td>Melt</td>
| |
| - | <td>35 cycles</td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 2</td>
| |
| - | <td> </td>
| |
| - | <td>25 sec</td>
| |
| - | <td>Anneal</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Cycle 3</td>
| |
| - | <td>72°C</td>
| |
| - | <td>30 sec per kb</td>
| |
| - | <td>Extend</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Finish</td>
| |
| - | <td>72 °C</td>
| |
| - | <td>5 min</td>
| |
| - | <td>Extand</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | <tr>
| |
| - | <td>Store</td>
| |
| - | <td>10°C</td>
| |
| - | <td>Forever</td>
| |
| - | <td>Store</td>
| |
| - | <td> </td>
| |
| - | </tr>
| |
| - | </table><br>
| |
| - | <br>
| |
| - | <b>Liquid culture of pS004’ and pS013’</b>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_1st_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 1<sup>st</sup> October</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Miniprep
| |
| - | pS013’, pS004’
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | 1) Pellet liquid culture (4000rpm, 10 min)<br>
| |
| - | 2) Discard supernatant<br>
| |
| - | 3) resuspend the cells in 250ul of resuspension olution<br>
| |
| - | 4) add 250ul of lysis solution, mix by inverting 4-6 times<br>
| |
| - | 5) add 350ul of neutralization solution<br>
| |
| - | 4) centrifuge for 5 min<br>
| |
| - | 5) transfer supernatant to spin column<br>
| |
| - | 6) centrifuge for 1 min<br>
| |
| - | 7) discard flow through<br>
| |
| - | 8) add 500 ul wash solution and centrifuge for 1 min , discard flow through(repeat this step)<br>
| |
| - | 9) centrifuge for 1 min to remove left over liquid<br>
| |
| - | 10) transfer the column on a 1.5ml tube<br>
| |
| - | 11) add 50ul of elution buffer and incubate for 2 min<br>
| |
| - | 12) centrifuge for 2 min<br>
| |
| - | 13) Nanodrop the concentration and freeze at -20°<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_2nd_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3> Wednesday 2<sup>nd</sup> October</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Preparation killing assay
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <br>
| |
| - | <b>Liquid cultures</b><br>
| |
| - | R16, R26, R26f, delta PyrF, parental delta PyrF, NEB, M13, Litmus + Helper, Litmus GFP + helper
| |
| - | <html><div id="detect_Thursday_3rd_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wedsnesday 3<sup>rd</sup> October</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Killing assay to test specifity of CRISPR Cas
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <b>Electrocompetent cells (delta PyrF, parental, NEB)</b>
| |
| - | <br>
| |
| - | 1) Start Culture
| |
| - | <br>
| |
| - | 2) When the cells reach an OD600 of 0.2.
| |
| - | <br>
| |
| - | 3) Harvest the cells.
| |
| - | <br>
| |
| - | When the cells reach an OD600 of between 0.6 and 0.8 (OD: 0,683)
| |
| - | <br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.
| |
| - | <br>
| |
| - | 4) Wash and combine the cells.
| |
| - | <br>
| |
| - | Remove the supernatant.
| |
| - | <br>
| |
| - | Resuspend the cells in 25 ml of ice cold water
| |
| - | <br>
| |
| - | 5) Wash the cells 2 more times.
| |
| - | <br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.
| |
| - | <br>
| |
| - | Resuspend in 50 ml of ice cold water.
| |
| - | <br>
| |
| - | Repeat.
| |
| - | <br>
| |
| - | 6) Wash and concentrate the cells for electroporation.
| |
| - | <br>
| |
| - | Centrifuge at 4 °C for 10 min at 4000 rpm.
| |
| - | <br>
| |
| - | Resuspend in 1-2 ml of ice cold water.
| |
| - | <br>
| |
| - | We will use 200 ul of washed cells per transformation.
| |
| - | <br>
| |
| - | <br>
| |
| - | <b>Transformation </b>
| |
| - | <br>
| |
| - | Cotransform into parental/keio delta pyRF: pS006* (Cas9 in Amp BB) + pS004'(gRNA in Chl BB).<br>
| |
| - | 1) Prepare BD tubes with a pipette filled with LB at the interior of each tube (pipette supplied with the electroporation cuvette)
| |
| - | <br>
| |
| - | 2) Test the purity of the electrocompetent cells.
| |
| - | <br>
| |
| - | Add 200 ul of washed cells to a cuvette.
| |
| - | <br>
| |
| - | 3) Mix the cells and DNA in a cuvette.
| |
| - | <br>
| |
| - | 200 ul of washed cells with 200 ng of PCR product.
| |
| - | <br>
| |
| - | Keep the cuvette on ice until just before the electroporation.
| |
| - | <br>
| |
| - | 4) Preload a pipette with 1 ml of LB.
| |
| - | <br>
| |
| - | 5) Pulse the cuvette with voltage.
| |
| - | <br>
| |
| - | Dry the electrodes with a kimwipe prior to loading.
| |
| - | <br>
| |
| - | Use the EC2 setting.
| |
| - | <br>
| |
| - | 6) Listen for arcing.
| |
| - | <br>
| |
| - | A cracking sound means all the cells are dead.
| |
| - | <br>
| |
| - | Note the time constant: 5 is good, 5.8 is great.
| |
| - | <br>
| |
| - | 7) Immediately recover the cells.
| |
| - | <br>
| |
| - | Add the 1 ml of preloaded LB and pipet up and down to mix.
| |
| - | <br>
| |
| - | Collect 1 ml of cells, some volume is lost in the cuvette.
| |
| - | <br>
| |
| - | 8) Incubate 1/2 h at 37 °C with shaking.
| |
| - | <br>
| |
| - | 9) Plate 10/200 ul of recovered cells on selective plates.
| |
| - | <br>
| |
| - | Use antibiotic appropriate to the part being integrated.
| |
| - | <br>
| |
| - | Let the other 900 ul rest overnight at room temperature.
| |
| - | <br>
| |
| - | 10) Concentrate and plate the remaining cells
| |
| - | <br>
| |
| - | Spin down quickly and resuspend in 100 ul LB before plating.
| |
| - | <br>
| |
| - | Transformed cells should be incubated at 37 °C.
| |
| - | <br>
| |
| - | Colonies should appear 24-48 h after plating.
| |
| - | <br>
| |
| - |
| |
| - | <br>
| |
| - | <br>
| |
| - | Plating of 10/100ul on <br>
| |
| - | 1. Amp plates -> selection for only Cas9<br>
| |
| - | 2. Chl plates -> selection for only gRNA<br>
| |
| - | 3. Amp/Chl plates -> selection for theoretically functional system<br>
| |
| - |
| |
| - | <html><div id="detect_Monday_14th_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Monday 14<sup>th</sup> October</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Liquid cultures sSP008, sSP009, R16, R26, R26f, sT007, sSP021, SCPR2-A3, SPCE2-C3
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Tuesday_15th_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 15<sup>th</sup> October</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Digestion Reporter and SPCR3
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | BB: SpeI, PstI<br>
| |
| - | SPCR: XbaI, PstI<br>
| |
| - | 2h 37°, heat inactivation<br>
| |
| - | <br>
| |
| - | Electrocompetent cells: sSP008, sSP009<br>
| |
| - | Transform SPCR2-A3/C3 both into sSP008/9<br>
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Wednesday_16th_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Wednesday 16<sup>th</sup> October</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Miniprep of pS002, pS002’, pS006*
| |
| - | Liquid culture sSP017, pS004, pS004’
| |
| - | Glycerols
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - |
| |
| - | <!-- === To here === -->
| |
| - | </div>
| |
| - | </html>
| |
| - | <html><div id="detect_Thursday_17th_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 17<sup>th</sup> October</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
| |
| - | Place your twit here
| |
| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | Miniprep sSP017, pS004, pS004’<br>
| |
| - | <br>
| |
| - | Digest Litmus pS018 EcoRI/PstI, EcoRI/XbaI 2h 37° shaking<br>
| |
| - | <br>
| |
| - | PCR purify<br>
| |
| - | <br>
| |
| - | Ligation:<br>
| |
| - | 1. gRNA+phagmid (10,4+6)<br>
| |
| - | 2.phagemid+gRNA+reporter (9,6+1,86+2)<br>
| |
| - | 3.phagemid+gRNA+Cas9 (10,2+2,04+3)<br>
| |
| - | <br>
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| - | 1h at 22°<br>
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| - | <br>
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| - | Transform<br>
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| - | Heat shock, cells matt<br>
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| - | Recover, plate<br>
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| - | </html>
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| - | <html><div id="detect_Friday_18th_October.html"</div></html>
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| - | <html>
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| - | <div class ="tbnote">
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| - | <h2>Detect</h2>
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| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
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| - | <div style="clear: both;"></div>
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| - | <h3>Friday 18<sup>th</sup> October</h3>
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| - | <p><b><em>
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| - | <!-- === Modify from here === -->
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| - | Miller assay and Liquid phagemid
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| - | <!-- === To here === -->
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| - | </br></em></b></p>
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| - | <!-- === Modify from here === -->
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| - | Place your note here
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| - | <!-- === To here === -->
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| - | </div>
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| - | </html>
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| - | <html><div id="detect_Saturday_19th_October.html"</div></html>
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| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
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| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
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| - | <div style="clear: both;"></div>
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| - | <h3>Saturday 19<sup>th</sup> October</h3>
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| - | <p><b><em>
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| - | <!-- === Modify from here === -->
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| - |
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| - | <!-- === To here === -->
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| - | </br></em></b></p>
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| - | <!-- === Modify from here === -->
| |
| - | <b>Miller<br>
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| - | Miniprerp phagemid<br>
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| - | Digest phagemid E/P, E/X, SPCR3 E,P<br></b>
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| - | <!-- === To here === -->
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| - | </div>
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| - | </html>
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| - |
| |
| - | <html><div id="detect_Tuesday_22nd_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Tuesday 22<sup>nd</sup> October</h3>
| |
| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
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| - | Liquid for Miller and Digest&purify SPCR3 E,P
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| - | <!-- === To here === -->
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| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
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| - |
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| - | <!-- === To here === -->
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| - | </div>
| |
| - | </html>
| |
| - |
| |
| - | <html><div id="detect_Thursday_24th_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Thursday 24<sup>th</sup> October</h3>
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| - | <p><b><em>
| |
| - | <!-- === Modify from here === -->
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| - |
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| - | <!-- === To here === -->
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| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Digest phagemid E/P</b><br>
| |
| - | Purify it<br>
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| - | <br>
| |
| - | <b>Ligation:</b><br>
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| - | 1. SPCR3 E/P + phagemid E/P<br>
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| - | 2. SPCR3 E/P + SPCR5 P/X+ phagemid E/X<br>
| |
| - | 2. SPCR3 E/P + SPCR2 P/X+ phagemid E/X<br>
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| - | <br>
| |
| - | <b>trafo Ligations<br>
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| - | <br>
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| - | electrocmpetent cells parental+sSP009+pS002’<br>
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| - | trafo:</b><br>
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| - | 1. parental+pS002<br>
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| - | 2. parental+pS002’<br>
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| - | 3. parental+pS006*<br>
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| - | 4. parental+pS002’+pS006*<br>
| |
| - | 5. sSP009 pS002’ + pS006*<br>
| |
| - | <br>
| |
| - | trafo helper into NEB<br>
| |
| - | <br>
| |
| - | liquid cultures: sSP009, pRECA strains Ariel, sSP008+pS002, sSP008+pS002’
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| - |
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| - | <!-- === To here === -->
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| - | </div>
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| - | </html>
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| - | <html><div id="detect_Friday_25th_October.html"</div></html>
| |
| - | <html>
| |
| - | <div class ="tbnote">
| |
| - | <h2>Detect</h2>
| |
| - | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/Detect" target="_blank" class="tbnotelogo PSlogo"> ASDF </a>
| |
| - | <div style="clear: both;"></div>
| |
| - | <h3>Friday 25<sup>th</sup> October</h3>
| |
| - | <p><b><em>
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| - | <!-- === Modify from here === -->
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| - |
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| - | <!-- === To here === -->
| |
| - | </br></em></b></p>
| |
| - | <!-- === Modify from here === -->
| |
| - | <b>Colony PCR<br>
| |
| - | Liquid Cloning</b><br>
| |
| - | <br>
| |
| - | Liquid: NEB helper, parental pS002, parental pS006*, sSP008+pS002, sSP008+pS002’<br>
| |
| - | <br>
| |
| - | Trafo: NEB helper+phageid-gRNA, parental ps006*+pS002’, pyrfF F+ pS002’+pS006*<br>
| |
| - | <br>
| |
| - | conjugation of parental pS006* with pS009<br>
| |
| - | <br>
| |
| - | Miniprep phagemid gRNA<br>
| |
| - | <br>
| |
| - | Liquid library<br>
| |
| - | Restreak for library<br>
| |
| - | <br>
| |
| - | <br>
| |
| - | 1) sSP008+pS002/pS002’ +Xgal<br>
| |
| - | 2) sSP008+pS002/pS002’ +Xgal + MMC<br>
| |
| - | 3) sSP008+pS002/pS002’ +MMC<br>
| |
| - |
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| - | <!-- === To here === -->
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| - | </div>
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| - | </html>
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| - |
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| - | </div>
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| - | </div>
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| - | <div style="clear: both;"></div>
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| - |
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| - | </html>
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| - |
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| - | {{:Team:Paris_Bettencourt/footer}}
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