Team:Caltech/week7

From 2014.igem.org

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<b>lamBCDA & fsrABC Reception Systems</b>
<b>lamBCDA & fsrABC Reception Systems</b>
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<ul><li>Single-transformations run on each of the constructs used in the double-transformations:
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    <ol><li>pMB001</li><li>pMB002</li><li>pMB003</li><li>pMB004</li><li>pMB005</li><li>pMB006</li></ol></li>
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<b>agrBCDA Reception System and Combinatorial Promoters</b>
<b>agrBCDA Reception System and Combinatorial Promoters</b>
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<b>lamBCDA & fsrABC Reception Systems</b>
<b>lamBCDA & fsrABC Reception Systems</b>
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<ul>
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<ul><li>Colony PCR was run on several of the colonies that emerged from the single-transformations last night</li>
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    <li>Gel was run, but wrong primers were used. New primers for sequencing/colPCR were ordered, and colPCR will be redone tomorrow.</li>
</ul>
</ul>
<b>agrBCDA Reception System and Combinatorial Promoters</b>
<b>agrBCDA Reception System and Combinatorial Promoters</b>

Revision as of 21:50, 29 July 2014
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Notebook
Overview

Week 1

Week 2

Week 3

Week 4

Week 5

Week 6

Week 7

Week 8

Week 9

Week 10

Week 11

Week 12

Week Seven

Monday, 7/28/14

 Export Systems
  • Ran colony PCR on pTG002/3/6-transformed JM109 cultures grown up over the weekend. Bad results for all of them
  • Created and ordered new primers that will hopefully avoid secondary-structure-formation when the exonuclease attacks the 5' end during Gibson assembly.
lamBCDA & fsrABC Reception Systems
  • Single-transformations run on each of the constructs used in the double-transformations:
    1. pMB001
    2. pMB002
    3. pMB003
    4. pMB004
    5. pMB005
    6. pMB006
agrBCDA Reception System and Combinatorial Promoters
  • Colonies were picked from pAA008 transformations incubated over the weekend, as well as the pAA009 & pAA010 transformations, which had been set up last Thursday.
  • Set up liquid cultures of the colonies to grow overnight in preparation for miniprep and sequencing tomorrow

Tuesday, 7/29/14

 Export Systems
lamBCDA & fsrABC Reception Systems
  • Colony PCR was run on several of the colonies that emerged from the single-transformations last night
  • Gel was run, but wrong primers were used. New primers for sequencing/colPCR were ordered, and colPCR will be redone tomorrow.
agrBCDA Reception System and Combinatorial Promoters

Wednesday, 7/30/14

 Export Systems
lamBCDA & fsrABC Reception Systems
agrBCDA Reception System and Combinatorial Promoters

Thursday, 7/31/14

 Export Systems
lamBCDA & fsrABC Reception Systems
agrBCDA Reception System and Combinatorial Promoters

Friday, 8/1/14

 Export Systems
lamBCDA & fsrABC Reception Systems
agrBCDA Reception System and Combinatorial Promoters

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