Team:Paris Saclay/Notebook/July/10

From 2013.igem.org

(Difference between revisions)
(Lab work)
(Notebook : July 10)
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For regulation system:
For regulation system:
*prepared the solution of BioBrick fnr repressor in PsB1C3 plasmid for DNA sequencing.
*prepared the solution of BioBrick fnr repressor in PsB1C3 plasmid for DNA sequencing.
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*the terminator transformation of yesterday did not work, a second transformation had been done for it.
+
*the terminator transformation of BBa_B0010 did not work yesterday, a second transformation had been done for it.
*The transformation for RBS+LacZ+terminator plasmid into competent cells was performed.
*The transformation for RBS+LacZ+terminator plasmid into competent cells was performed.
*after the transformation PSB3K3 plasmid in competent cells, these cells were cultured in a liquid nutritive medium.
*after the transformation PSB3K3 plasmid in competent cells, these cells were cultured in a liquid nutritive medium.
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=='''Lab work'''==
=='''Lab work'''==
A.aero/anaerobic regulation system
A.aero/anaerobic regulation system
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::BioBrick RBS+LacZ+terminator in plasmid PSB1C3
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:BioBrick RBS+LacZ+terminator in plasmid PSB1C3
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::BioBrick RBS+amilCP+terminator in plasmid PSB1C3  
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:BioBrick RBS+amilCP+terminator in plasmid PSB1C3  
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<u>Transformation</u>
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<p>Transformation for BBa_B0010 dit work, we observed 0 colonies on the Petri dish, We decided to redo another transformation</p>
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 +
<p>Transformation for BBa_I732019(RBS+LacZ+terminator BBa_B0010):
 +
:the construction of RBS+LacZ+terminator BBa_B0010 is already done and stocked in iGEM BioBrick bank named BBa_I732019 12G p4 kit 2012. So we just suspended the BioBrick with 10µl water, transformed them into 100µl competent cell.</p>
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 +
<p>Cloning for plasmid PSB3K3:
 +
:results of transformation and cloning: 34 colonies grown.
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:We picked up 2 colonies, seeded them in liquid medium(LB+cchloramphenicol), incubation at 37°C, 200rpm during one night.</p>
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Revision as of 15:03, 21 September 2013

Notebook : July 10

Summary:

For regulation system:

  • prepared the solution of BioBrick fnr repressor in PsB1C3 plasmid for DNA sequencing.
  • the terminator transformation of BBa_B0010 did not work yesterday, a second transformation had been done for it.
  • The transformation for RBS+LacZ+terminator plasmid into competent cells was performed.
  • after the transformation PSB3K3 plasmid in competent cells, these cells were cultured in a liquid nutritive medium.


For PSBs sensor system:

  • the ligation products were transformed into competent cells and were cultured on solid medium with their specific antibiotics.

Lab work

A.aero/anaerobic regulation system

BioBrick RBS+LacZ+terminator in plasmid PSB1C3
BioBrick RBS+amilCP+terminator in plasmid PSB1C3

Transformation

Transformation for BBa_B0010 dit work, we observed 0 colonies on the Petri dish, We decided to redo another transformation

Transformation for BBa_I732019(RBS+LacZ+terminator BBa_B0010):

the construction of RBS+LacZ+terminator BBa_B0010 is already done and stocked in iGEM BioBrick bank named BBa_I732019 12G p4 kit 2012. So we just suspended the BioBrick with 10µl water, transformed them into 100µl competent cell.

Cloning for plasmid PSB3K3:

results of transformation and cloning: 34 colonies grown.
We picked up 2 colonies, seeded them in liquid medium(LB+cchloramphenicol), incubation at 37°C, 200rpm during one night.


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