Team:Paris Saclay/Notebook/July/10
From 2013.igem.org
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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