http://2010.igem.org/wiki/index.php?title=Team:Calgary/22_October_2010&feed=atom&action=historyTeam:Calgary/22 October 2010 - Revision history2024-03-28T20:49:49ZRevision history for this page on the wikiMediaWiki 1.16.5http://2010.igem.org/wiki/index.php?title=Team:Calgary/22_October_2010&diff=170238&oldid=prevH.dastidar at 01:06, 27 October 20102010-10-27T01:06:51Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>This morning Chris and I went to Churchill High School where we did a presentation at their Science Cafe. We talked a bit about Synthetic Biology, iGEM and a bit about our project in general. The students seemed quite interested and we had a ton of questions about iGEM and various iGEM projects. This afternoon I made competant cells with the ibpAB-I13504 plasmid in them. We made both electrocompetant cells as well as chemically competant Calcium chloride cells. Today we also constructed all of the registry parts that we want to submit into the psB1C3 vector. After digestion and Antarctic Phosphotase treatment of the vector, I ligated, transformed into TOP10 E. Coli cells and then plated on Chloramphenicol plates. Today we also spent a fair bit of time looking into what functional testing has been done on our system up to date and deciding what more needs to be accomplished over the next few days and how we are ging to do that.</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>This morning Chris and I went to Churchill High School where we did a presentation at their Science Cafe. We talked a bit about Synthetic Biology, iGEM and a bit about our project in general. The students seemed quite interested and we had a ton of questions about iGEM and various iGEM projects. This afternoon I made competant cells with the ibpAB-I13504 plasmid in them. We made both electrocompetant cells as well as chemically competant Calcium chloride cells. Today we also constructed all of the registry parts that we want to submit into the psB1C3 vector. After digestion and Antarctic Phosphotase treatment of the vector, I ligated, transformed into TOP10 E. Coli cells and then plated on Chloramphenicol plates. Today we also spent a fair bit of time looking into what functional testing has been done on our system up to date and deciding what more needs to be accomplished over the next few days and how we are ging to do that.</div></td></tr>
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<tr><td colspan="2"> </td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline">Today I did temperature readings for heat shock experiment with CpxR-I13507 cells. The idea behind this is to characterize our parts using established literature parameters. I read every hour for 5 hours starting from time zero.</ins></div></td></tr>
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</table>H.dastidarhttp://2010.igem.org/wiki/index.php?title=Team:Calgary/22_October_2010&diff=168775&oldid=prevEmily Hicks at 23:29, 26 October 20102010-10-26T23:29:39Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Friday October 22, 2010|</div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>Friday October 22, 2010|</div></td></tr>
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<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;"><u>Emily</u></ins></div></td></tr>
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<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;">This morning Chris and I went to Churchill High School where we did a presentation at their Science Cafe. We talked a bit about Synthetic Biology, iGEM and a bit about our project in general. The students seemed quite interested and we had a ton of questions about iGEM and various iGEM projects. This afternoon I made competant cells with the ibpAB-I13504 plasmid in them. We made both electrocompetant cells as well as chemically competant Calcium chloride cells. Today we also constructed all of the registry parts that we want to submit into the psB1C3 vector. After digestion and Antarctic Phosphotase treatment of the vector, I ligated, transformed into TOP10 E. Coli cells and then plated on Chloramphenicol plates. Today we also spent a fair bit of time looking into what functional testing has been done on our system up to date and deciding what more needs to be accomplished over the next few days and how we are ging to do that.</ins></div></td></tr>
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</table>Emily Hickshttp://2010.igem.org/wiki/index.php?title=Team:Calgary/22_October_2010&diff=105727&oldid=prevPjwu: New page: {{CalgaryNotebookTemplate| Friday October 22, 2010| }}2010-10-17T04:30:05Z<p>New page: {{CalgaryNotebookTemplate| Friday October 22, 2010| }}</p>
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