Team:Caltech/Week 4
From 2011.igem.org
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==July 4== | ==July 4== | ||
===Results=== | ===Results=== | ||
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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/> | ||
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Work on Project Description and Safety Proposal<br/> | Work on Project Description and Safety Proposal<br/> | ||
Once we've sequenced ER ([http://partsregitry.org/Part:BBa_K123003 K123003]), start making test plasmids to see if it works.</p> | Once we've sequenced ER ([http://partsregitry.org/Part:BBa_K123003 K123003]), start making test plasmids to see if it works.</p> | ||
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+ | ==July 5== | ||
+ | <p>Start overnight cultures of Gibson transformations</p> | ||
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+ | ==July 6== | ||
+ | <p>Miniprep Gibson transformations and send off for sequencing</p> | ||
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Revision as of 20:48, 5 July 2011
Project |
July 3Checked Gibson transformations ResultsThere 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. However, we have had trouble with our competent cells in the past and will try plating what we have left.
July 4ResultsAfter plating the remaining 450 ul of our transformed cells:
This WeekStart enrichment cultures from a previous iteration, as the latest dilutions remain clear. July 5Start overnight cultures of Gibson transformations July 6Miniprep Gibson transformations and send off for sequencing
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