Team:Paris Saclay/Notebook/July/8

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(Difference between revisions)
(→Lab work)
(→2 - Transformation in DH5α of the following biobricks:)
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* BBa J23114(AmpR
* BBa J23114(AmpR
* Control + : pUC18 (20ng)
* Control + : pUC18 (20ng)
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* control -  
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* Control -  
[https://2013.igem.org/Team:Paris_Saclay/Protocols/Transformation Protocol]
[https://2013.igem.org/Team:Paris_Saclay/Protocols/Transformation Protocol]
 +
 +
NB : The protocol was modified. Instead of spreading 10-1 and 10-2 solutions of bacteria we took a non diluted solution and a 10-1 solution.
===='''3 - Plasmid DNA preparation:'''====
===='''3 - Plasmid DNA preparation:'''====

Revision as of 15:07, 9 July 2014

Contents

Notebook : July 8

Lab work

1 - Rehydration of the following biobricks:

Sean

  • BBa B0015(CmR)
  • BBa J23119(CmR)
  • BBa K731020(CmR)
  • BBa K206000(CmR)
  • BBa J04500(CmR)
  • BBa J23100(AmpR)
  • BBa J23106(AmpR)
  • BBa J23114(AmpR)


Protocol:

  1. Pierce foil cover of well containing biobrick of interest.
  2. Add 10 μL of water in well.
  3. Transfer contents of well into a 1.5 mL microcentrifuge tube.

2 - Transformation in DH5α of the following biobricks:

Mathieu & Maher

  • BBa B0015(CmR)
  • BBa J23119(CmR)
  • BBa K731020(CmR)
  • BBa K206000(CmR)
  • BBa J04500(CmR)
  • BBa J23100(AmpR)
  • BBa J23106(AmpR)
  • BBa J23114(AmpR
  • Control + : pUC18 (20ng)
  • Control -


Protocol

NB : The protocol was modified. Instead of spreading 10-1 and 10-2 solutions of bacteria we took a non diluted solution and a 10-1 solution.

3 - Plasmid DNA preparation:

Romain & Sean

Plasmids used:

  • pJBEI-6409


E. coli strain used:

  • XL1-Blue
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