Team:Paris Saclay/Notebook/July/12

From 2013.igem.org

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Anaïs
Anaïs
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We strek 25 colonies of 07/10/13 transformation of BphA1 and BphR2 in new solid culture.  
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We streak 25 colonies of 07/10/13 transformation of BphA1 and BphR2 in new solid culture.  
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Revision as of 19:32, 26 September 2013

Contents

Notebook : July 12

Lab work

A - Aerobic/Anaerobic regulation system

Objective : obtaining Bba_K1155003, Bba_K1155007

1 -Transformation of Bba_I732019, Bba_B0015, Bba_B0017

Zhou

Transformation of 07/10/13 of Bba_I732019 didn't works. We will do it again.

Protocol : Bacterial transformation

2 -Design of RBS-AmilCP oligos

Abdou, Anaïs

We used software gene manager to find the correct oligopeptides for amplification of RBS-Amil CP.


B - PCB sensor system

Objective : obtaining Bba_K1155001, Bba_K1155002 and BphR2

1 - Stock of clones 5, 6, 7, 8 for Bba_K1155002, clones 5, 6 for Bba_K1155001 and clones 3, 4 for BphR2

Zhou

Used quantities :

  • Glycerol 85% : 425
  • Culture : 1µL

2 - Extraction of clones 5, 6, 7, 8 for Bba_K1155002, clones 5, 6 for Bba_K1155001 and clones 3, 4 for BphR2 from DH5α

Abdou, Sheng

Protocol : High copy plamid extraction

3 - Streak of Bba_K1155002 and BphR2

Anaïs

We streak 25 colonies of 07/10/13 transformation of BphA1 and BphR2 in new solid culture.


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