Team:Paris Saclay/Notebook/July/12

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(Difference between revisions)
(Lab work)
(Notebook : July 12)
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<u>Transformation</u>
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<p>We suspended the DNA with water from iGEM plate and performed several transformation.</p><br>
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*BBa_I732019: LacZ+RBS+terminator into plasmid BBa_I732950(ampicillin resitant).
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*BBa_B0015: 2 terminators BBa_B0010+BBa_B0012(4F plate 3 kit 2013) into plasmid PSB1C3.
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*BBa_B0017: 2 terminators BBa_B0010+BBa_B0010 into plasmid PSB1C3.
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*Simple terminator BBa_B0010 into plasmid PSB1A2.
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see protocol Tranformation.
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B.PCBs sensor system:
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<p>The stock and extraction of promoter BphR1 clone 5 and 6, promoter BphR2 clone 3 and 4, promoter BphA1 clone 5 to 8 performed according to protocol. Please see protocol DNA extraction and sample stock.</p>
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Revision as of 02:26, 22 September 2013

Notebook : July 12

summary

For fnr regulator system:

  • Performed 4 transformations(3 terminator and 1 RBS+LacZ+terminator into competent cells).
  • Design of oligo for amplifying AmiCP+RBS.

For PCBs sensor system:

  • Had the promoter BphR1 clone 5 and 6, promoter BphR2 clone 3 and 4, promoter BphA1 clone 5 to 8 in stock.
  • Plasmid DNA extraction from promoter BphR1 clone 5 and 6, promoter BphR2 clone 3 and 4, promoter BphA1 clone 5 to 8.

Lab work

A.aero/anaerobic regulation system:

  • BioBrick RBS+LacZ+terminator in plasmid PSB1C3


Transformation

We suspended the DNA with water from iGEM plate and performed several transformation.


  • BBa_I732019: LacZ+RBS+terminator into plasmid BBa_I732950(ampicillin resitant).
  • BBa_B0015: 2 terminators BBa_B0010+BBa_B0012(4F plate 3 kit 2013) into plasmid PSB1C3.
  • BBa_B0017: 2 terminators BBa_B0010+BBa_B0010 into plasmid PSB1C3.
  • Simple terminator BBa_B0010 into plasmid PSB1A2.

see protocol Tranformation.

B.PCBs sensor system:

The stock and extraction of promoter BphR1 clone 5 and 6, promoter BphR2 clone 3 and 4, promoter BphA1 clone 5 to 8 performed according to protocol. Please see protocol DNA extraction and sample stock.


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