Team:Caltech/Week 4

From 2011.igem.org

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Content=
Content=
__NOTOC__
__NOTOC__
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==July 3==
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===Results===
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There was no growth on the transformed Gibson plates. Since we did a small reaction, we used all of the reaction in transforming competent cells. The Gibson assembly likely failed, as one of the negative control plates had a single colony.<br/><br/>
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Gibson Transformations
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<table border="1">
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<tr>
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<th>Plate</th>
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<th>Number of Colonies</th>
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</tr>
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<tr>
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<td>pNT001 +</td>
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<td>0</td>
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</tr>
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<tr>
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<td>pNT001 -</td>
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<td>0</td>
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</tr>
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<tr>
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<td>pNT002 +</td>
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<td>0</td>
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</tr>
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<tr>
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<td>pNT002 -</td>
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<td>1</td>
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</tr>
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</table>
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==This Week==
==This Week==
<p>Start enrichment cultures from a previous iteration, as the latest dilutions remain clear.<br/>
<p>Start enrichment cultures from a previous iteration, as the latest dilutions remain clear.<br/>

Revision as of 18:05, 3 July 2011


Caltech iGEM 2011



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July 3

Results

There was no growth on the transformed Gibson plates. Since we did a small reaction, we used all of the reaction in transforming competent cells. The Gibson assembly likely failed, as one of the negative control plates had a single colony.

Gibson Transformations

Plate Number of Colonies
pNT001 + 0
pNT001 - 0
pNT002 + 0
pNT002 - 1

This Week

Start enrichment cultures from a previous iteration, as the latest dilutions remain clear.
Design experiments to test for degradation of BPA by pNT001 and pNT002 using the HPLC
Get the BioBricks we ordered from the parts registry ([http://partsregistry.org/Part:BBA_K364309 K364309], [http://partsregistry.org/Part:BBA_K364329 K364329], [http://partsregistry.org/Part:BBA_K364327 K364327], [http://partsregistry.org/Part:BBA_K364307 K364307])
Transform these into cells, miniprep and sequence
Continue with enrichment cultures
Put LA River soil DNA into fosmids
Work on Project Description and Safety Proposal
Once we've sequenced ER ([http://partsregitry.org/Part:BBa_K123003 K123003]), start making test plasmids to see if it works.


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