http://2013.igem.org/wiki/index.php?title=Team:Groningen/9_July_2013&feed=atom&action=historyTeam:Groningen/9 July 2013 - Revision history2024-03-29T09:51:39ZRevision history for this page on the wikiMediaWiki 1.16.5http://2013.igem.org/wiki/index.php?title=Team:Groningen/9_July_2013&diff=28695&oldid=prevInne at 09:19, 11 July 20132013-07-11T09:19:33Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>''' Inne'''</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>''' Inne'''</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>spotted <del class="diffchange diffchange-inline">transmuted </del>cells and put them in a 37 C shaker (at 11:35)</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>spotted <ins class="diffchange diffchange-inline">transformed </ins>cells and put them in a 37 C shaker (at 11:35)</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Cells need to grow over night.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Cells need to grow over night.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>15:00 PCR in order to get more silk gene to cut out of gel(last one was cut to low)</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>15:00 PCR in order to get more silk gene to cut out of gel(last one was cut to low)</div></td></tr>
</table>Innehttp://2013.igem.org/wiki/index.php?title=Team:Groningen/9_July_2013&diff=26993&oldid=prevInne at 13:03, 9 July 20132013-07-09T13:03:34Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>spotted transmuted cells and put them in a 37 C shaker (at 11:35)</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>spotted transmuted cells and put them in a 37 C shaker (at 11:35)</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;">Cells need to grow over night.</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;">15:00 PCR in order to get more silk gene to cut out of gel(last one was cut to low)</ins></div></td></tr>
</table>Innehttp://2013.igem.org/wiki/index.php?title=Team:Groningen/9_July_2013&diff=26979&oldid=prevMirjam at 12:35, 9 July 20132013-07-09T12:35:02Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>Gel run for 22 min 90V.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>Gel run for 22 min 90V.</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>Gel reveals a small band at 900bp. That is why a new 1.5% agarosegel is run for 30 min at 90V.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>Gel reveals a small band at 900bp. That is why a new 1.5% agarosegel is run for 30 min at 90V.</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"><br/>Cut wrong bands from gel. So a new PCR is made.</ins></div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>''' Inne'''</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>''' Inne'''</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>spotted transmuted cells and put them in a 37 C shaker (at 11:35)</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>spotted transmuted cells and put them in a 37 C shaker (at 11:35)</div></td></tr>
</table>Mirjamhttp://2013.igem.org/wiki/index.php?title=Team:Groningen/9_July_2013&diff=26868&oldid=prevMirjam at 09:56, 9 July 20132013-07-09T09:56:39Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>PCR made for silk without strep-tags. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>PCR made for silk without strep-tags. </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>Gel run for 22 min 90V.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>Gel run for 22 min 90V.</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"><br/>Gel reveals a small band at 900bp. That is why a new 1.5% agarosegel is run for 30 min at 90V.</ins></div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>''' Inne'''</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>''' Inne'''</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>spotted transmuted cells and put them in a 37 C shaker (at 11:35)</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>spotted transmuted cells and put them in a 37 C shaker (at 11:35)</div></td></tr>
</table>Mirjamhttp://2013.igem.org/wiki/index.php?title=Team:Groningen/9_July_2013&diff=26831&oldid=prevInne at 09:39, 9 July 20132013-07-09T09:39:01Z<p></p>
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<td colspan='2' style="background-color: white; color:black;">Revision as of 09:39, 9 July 2013</td>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>PCR made for silk without strep-tags. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>PCR made for silk without strep-tags. </div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>Gel run for 22 min 90V.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div><br/>Gel run for 22 min 90V.</div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;">''' Inne'''</ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins style="color: red; font-weight: bold; text-decoration: none;">spotted transmuted cells and put them in a 37 C shaker (at 11:35)</ins></div></td></tr>
</table>Innehttp://2013.igem.org/wiki/index.php?title=Team:Groningen/9_July_2013&diff=26800&oldid=prevMirjam: Created page with "'''Mirjam''' <br/>PCR made for silk without strep-tags. <br/>Gel run for 22 min 90V."2013-07-09T09:17:37Z<p>Created page with "'''Mirjam''' <br/>PCR made for silk without strep-tags. <br/>Gel run for 22 min 90V."</p>
<p><b>New page</b></p><div>'''Mirjam'''<br />
<br/>PCR made for silk without strep-tags. <br />
<br/>Gel run for 22 min 90V.</div>Mirjam