Latest revision as of 16:46, 30 August 2013

Week 13

Monday

Many gels were run to check the validity of our results. We discovered that our gene number four ligation was not sucessful and we would have to repeat the ligation of that particular gene. We also ligated the L-arabinose promoters to the pump or GFP. This was done with the three strengths of the promoters: strong, medium, and weak.

Tuesday

The L-arabinose promoters (strong, medium, weak) were transformed with the GFP or the pump into E.coli for testing. These plates were then put in the incubator and should be checked tomorrow! We hope to see colonies and then check to see if the expression corresponds with the strength of the promoter.

Wednesday

The plates were checked, and unfortunately, no colonies were found. The plates were left in the incubator to see if more time would allow for growth.

Thursday

The plates were checked again, and no growth was found. We decided that this must mean either our transformation or ligation of these parts was not successful.

Friday

The lab was cleaned and our boxes were placed in storage. The title and abstract forms were also completed.

@@ Line 4: / Line 4: @@
 <br><FONT color = 'green' size="+20">Week 13</FONT><BR><BR>
    <H1 align = left>Monday</H1>
-   <p style="text-align:justify">Text goes here.</p><br>
+   <p style="text-align:justify">Many gels were run to check the validity of our results. We discovered that our gene number four ligation was not sucessful and we would have to repeat the ligation of that particular gene. We also ligated the L-arabinose promoters to the pump or GFP. This was done with the three strengths of the promoters: strong, medium, and weak.</p><br>
    <H1 align = left>Tuesday</H1>
-   <p style="text-align:justify">Text goes here.</p><br>
+   <p style="text-align:justify">The L-arabinose promoters (strong, medium, weak) were transformed with the GFP or the pump into E.coli for testing. These plates were then put in the incubator and should be checked tomorrow! We hope to see colonies and then check to see if the expression corresponds with the strength of the promoter.</p><br>
    <H1 align = left>Wednesday</H1>
-   <p style="text-align:justify">Text goes here.</p><br>
+   <p style="text-align:justify">The plates were checked, and unfortunately, no colonies were found. The plates were left in the incubator to see if more time would allow for growth.</p><br>
    <H1 align = left>Thursday</H1>
-   <p style="text-align:justify">Text goes here.</p><br>
+   <p style="text-align:justify">The plates were checked again, and no growth was found. We decided that this must mean either our transformation or ligation of these parts was not successful. </p><br>
    <H1 align = left>Friday</H1>
-   <p style="text-align:justify">Text goes here.</p><br>
+   <p style="text-align:justify">The lab was cleaned and our boxes were placed in storage. The title and abstract forms were also completed. </p><br>
   </body>
 </html>
 {{Team:MSOE:Notebook}}

Team:MSOE Milwaukee/Week13

From 2013.igem.org