Team:Caltech/Week 3

From 2011.igem.org

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== June 27 ==
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==June 26==
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<p>lab</p>
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<p> Start overnight cultures of T7 polymerase ([http://partsregistry.org/Part:BBa_K145001 K145001]), mCherry ([http://partsregistry.org/Part:BBa_J06702 J06702]), Lac Promoter ([http://partsregistry.org/Part:BBa_R0010 R0010]), double terminator ([http://partsregistry.org/Part:BBa_B0014 B0014] and [http://partsregistry.org/Part:BBa_B0015 B0015]) and Tet Promoter ([http://partsregistry.org/Part:BBa_R0040 R0040])<br/>
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Transfer 0.5 mL aliquots of BPA and 5 mL aliquots 17a-ethynylestradiol cultures from June 23 to fresh minimal media</p>
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== This Week ==
 +
<p>Ethanol precipitation of DNA extractions from LA river samples<br/>
 +
Miniprep of T7 polymerase ([http://partsregistry.org/Part:BBa_K145001 K145001]), mCherry ([http://partsregistry.org/Part:BBa_J06702 J06702]), Lac Promoter ([http://partsregistry.org/Part:BBa_R0010 R0010]), double terminator ([http://partsregistry.org/Part:BBa_B0014 B0014] and [http://partsregistry.org/Part:BBa_B0015 B0015]) and Tet Promoter ([http://partsregistry.org/Part:BBa_R0040 R0040]) and submit for sequencing<br/>
 +
PCR of parts for pNT001 (Test plasmid for [http://partsregistry.org/Part:BBa_K123000 K123000])<br/>
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Purification/Gibson assembly for pNT001<br/>
 +
Cutting LA River DNA for insertion into fosmids<br/>
 +
Email other teams <br/>
 +
Insert LA River DNA into fosmids <br/>
 +
Transform fosmids into E. coli and start enrichment cultures<br/>
 +
Continue gene fishing <br/>
 +
Send off continued forward sequencing for HER<br/>
 +
PCR of parts for pNT002 and assembly<br/>
 +
Use pNT001 and pNT002 to test degradation parts</p>
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Revision as of 00:30, 25 June 2011


Caltech iGEM 2011



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June 26

Start overnight cultures of T7 polymerase (K145001), mCherry (J06702), Lac Promoter (R0010), double terminator (B0014 and B0015) and Tet Promoter (R0040)
Transfer 0.5 mL aliquots of BPA and 5 mL aliquots 17a-ethynylestradiol cultures from June 23 to fresh minimal media

This Week

Ethanol precipitation of DNA extractions from LA river samples
Miniprep of T7 polymerase (K145001), mCherry (J06702), Lac Promoter (R0010), double terminator (B0014 and B0015) and Tet Promoter (R0040) and submit for sequencing
PCR of parts for pNT001 (Test plasmid for K123000)
Purification/Gibson assembly for pNT001
Cutting LA River DNA for insertion into fosmids
Email other teams
Insert LA River DNA into fosmids
Transform fosmids into E. coli and start enrichment cultures
Continue gene fishing
Send off continued forward sequencing for HER
PCR of parts for pNT002 and assembly
Use pNT001 and pNT002 to test degradation parts


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