ULB/26 August 2010

From 2010.igem.org

(Difference between revisions)
Line 4: Line 4:
*Made the minipreps again.
*Made the minipreps again.
*First ligations of the various pieces to build the two plasmids.
*First ligations of the various pieces to build the two plasmids.
 +
 +
'''Module hydrogen'''
 +
* The test on the other deletion candidate are once again all negative
 +
* We continue the purification process for the deletion candidate
 +
* We continue to try to obtain other deletion candidates
 +
 +
'''Module homologous recombination'''
 +
* We inserted the cm and kan resistance cassette into the pSB1C3
 +
 +
'''Module heavy metals detection'''
 +
* We inserted the gene of the carotene behind a constitutive promoter, we let the bacteria grow
 +
* We inserted the copper sensitive promoter in front of a RFP, we let the bacteria grow
 +
 +
'''Other'''
 +
* We did a PCR on pSB1C3 in order to have some more

Revision as of 03:10, 28 October 2010

	
		

	
	
		
		
	

Quorum addiction module

  • The minipreps done on the 26 contained some genomic DNA, so we purified them on gel. Sadly, the purification didn't work, all the DNA was lost.
  • Made the minipreps again.
  • First ligations of the various pieces to build the two plasmids.

Module hydrogen

  • The test on the other deletion candidate are once again all negative
  • We continue the purification process for the deletion candidate
  • We continue to try to obtain other deletion candidates

Module homologous recombination

  • We inserted the cm and kan resistance cassette into the pSB1C3

Module heavy metals detection

  • We inserted the gene of the carotene behind a constitutive promoter, we let the bacteria grow
  • We inserted the copper sensitive promoter in front of a RFP, we let the bacteria grow

Other

  • We did a PCR on pSB1C3 in order to have some more