Team:Caltech/Notebook

From 2014.igem.org

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<tr><td colspan="3"> <h3>Notebook</h3></td></tr>
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<tr><td colspan="3"> <h3>Notebook</h3> Apparently there's a calendar feature to take care of this too???</td></tr>
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<tr><td colspan=3><h1>Week One</h1></td></tr>
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<p>You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well. </p>
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<h4>Tuesday, 6/17/14</h4>
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<ul><li>Get acquainted with summer logistics and lab basics</li>
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    <li>Clean up lab space, stock lab supplies</li>
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</ul>
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</td>
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<td>We got absolutely no results today!!!</td>
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<h4>Wednesday, 6/18/14</h4>
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<td width="40%" valign="top">
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<ul><li>Continue to discuss project and clean up lab space</li>
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    <li>Designed PCR primers for combinatorial promoters subproject</li>
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</ul>
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</td>
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<td>We got absolutely no results today!!!</td>
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<td width="20%"  valign="top">
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<h4>Thursday, 6/19/14</h4>
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<td width="40%" valign="top">
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<ul><li>Formulated plasmid design for the response regulation subproject</li>
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    <li>PCR plasmid backbone and sfGFP to create constructs with the proper overhangs for Gibson assembly</li>
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    <li>Gel electrophoresis for confirmation of PCR products' length</li>
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</ul>
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</td>
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<td>We got absolutely no results today!!!</td>
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</tr>
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<tr>
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<td width="20%"  valign="top">
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<h4>Friday, 6/20/14</h4>
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<ul><li>Purification of PCR products created yesterday</li>
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    <li>Gibson assembly of purified products</li>
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    <li>Transformation of Gibson-assembled plasmids into JM109 E. coli</li>
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    <li>Meeting with Prof. Murray to discuss give an update on the project</li>
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</ul>
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</td>
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<td>Colonies were found after transformation into </td>
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Revision as of 04:41, 23 June 2014



WELCOME TO iGEM 2014!

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Notebook

Apparently there's a calendar feature to take care of this too???

Week One

Tuesday, 6/17/14

  • Get acquainted with summer logistics and lab basics
  • Clean up lab space, stock lab supplies
We got absolutely no results today!!!

Wednesday, 6/18/14

  • Continue to discuss project and clean up lab space
  • Designed PCR primers for combinatorial promoters subproject
We got absolutely no results today!!!

Thursday, 6/19/14

  • Formulated plasmid design for the response regulation subproject
  • PCR plasmid backbone and sfGFP to create constructs with the proper overhangs for Gibson assembly
  • Gel electrophoresis for confirmation of PCR products' length
We got absolutely no results today!!!

Friday, 6/20/14

  • Purification of PCR products created yesterday
  • Gibson assembly of purified products
  • Transformation of Gibson-assembled plasmids into JM109 E. coli
  • Meeting with Prof. Murray to discuss give an update on the project
Colonies were found after transformation into