http://2010.igem.org/wiki/index.php?title=Team:Tsinghua/Notebook/8_August_2010&feed=atom&action=historyTeam:Tsinghua/Notebook/8 August 2010 - Revision history2024-03-28T11:26:09ZRevision history for this page on the wikiMediaWiki 1.16.5http://2010.igem.org/wiki/index.php?title=Team:Tsinghua/Notebook/8_August_2010&diff=141604&oldid=prevFanfan: /* Module I, DT and Fan's part: */2010-10-25T06:53:56Z<p><span class="autocomment">Module I, DT and Fan's part:</span></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>== Module I, <del class="diffchange diffchange-inline">DT and Fan's part: </del>==</div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>== Module I, <ins class="diffchange diffchange-inline">group 2(b) </ins>==</div></td></tr>
<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Using the 0.1% Amp LB to amplify the selected E.coli at 37℃ for at least 10h. For P+E and P+C, each one selects six colonies. </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Using the 0.1% Amp LB to amplify the selected E.coli at 37℃ for at least 10h. For P+E and P+C, each one selects six colonies. </div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Purify the plasmid 10 hours later.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Purify the plasmid 10 hours later.</div></td></tr>
</table>Fanfanhttp://2010.igem.org/wiki/index.php?title=Team:Tsinghua/Notebook/8_August_2010&diff=62959&oldid=prevFanfan: New page: == Module I, DT and Fan's part: == Using the 0.1% Amp LB to amplify the selected E.coli at 37℃ for at least 10h. For P+E and P+C, each one selects six colonies. Purify the plasmid 10 ...2010-09-03T09:48:21Z<p>New page: == Module I, DT and Fan's part: == Using the 0.1% Amp LB to amplify the selected E.coli at 37℃ for at least 10h. For P+E and P+C, each one selects six colonies. Purify the plasmid 10 ...</p>
<p><b>New page</b></p><div><br />
== Module I, DT and Fan's part: ==<br />
Using the 0.1% Amp LB to amplify the selected E.coli at 37℃ for at least 10h. For P+E and P+C, each one selects six colonies. <br />
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Purify the plasmid 10 hours later.</div>Fanfan