Team:Paris Saclay/Notebook/July/12
From 2013.igem.org
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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