Difference between revisions of "Team:Harvard/Notebook"

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        <a data-toggle="collapse" data-parent="#accordion" href="#collapse1">Week 1: 9/1 - 9/7</a>
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        We designed an RBS library for csgG using the <a href="https://salislab.net/software/">Salis Lab RBS Library Calculator<a>, as well as the appropriate PCR primers to construct the library and ordered these sequences from IDT.
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        <a data-toggle="collapse" data-parent="#accordion" href="#collapse2">Week 2: 9/8 - 9/14</a>
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      <div class="panel-body">Our DNA parts ordered the previous week arrived and we conducted PCRs with the primers we designed and a plasmid containing the sequences for csgA, csgB, csgC, csgE, csgF, and csgG obtained from the Joshi Lab to modify the RBS sequence in front of csgG. After verifying our PCR products with a gel, we used Gibson Assembly to put our cloned parts in an expression vector. </div>
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        <a data-toggle="collapse" data-parent="#accordion" href="#collapse3">Week 3: 9/15 - 9/21</a>
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      <div class="panel-body">No lab work :(</div>
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Revision as of 00:55, 1 November 2017

Harvard OPTI POLY

Lab Notebook


Week 1: 9/1 - 9/7

Week 2: 9/8 - 9/14

Our DNA parts ordered the previous week arrived and we conducted PCRs with the primers we designed and a plasmid containing the sequences for csgA, csgB, csgC, csgE, csgF, and csgG obtained from the Joshi Lab to modify the RBS sequence in front of csgG. After verifying our PCR products with a gel, we used Gibson Assembly to put our cloned parts in an expression vector.

Week 3: 9/15 - 9/21

No lab work :(