User:University of Washington/23 July 2008

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LuxR from AraC and TetR

- Miniprepped AraC R0080

- Results from Transformation of mutated AraC

  • Positive control : a lot of growth
  • Negative control : some growth (expected NO growth because primers weren't added.)
  • Reaction one : some growth
  • Reaction two : some growth

- Picked 4 colonies from each reaction and prepared overnight culture.

- Primers for Elowitz's promoter were designed and ordered.


Lambda Red Recombineering of RP4 (Bryan)

Troubleshooting of PCR continued. Attempted PCR on control template at 1.5 mM, 2 mM, 2.5 mM, and 3 mM magnesium chloride. No amplicon at 1.5 mM, which conflicts with results from yesterday's PCR. Best amplicon appeared at 2 mM. Since the results are inconsistent, it is difficult to optimize the reaction concentration based on this experiment.

Mini-prep of pSIM5 had no DNA in eluate. Putative error: pSIM5 does not have cam cassette leading to loss of plasmid or failure to grow in ON culture. Will not repeat mini-prep since pSIM5/host is in glycerol stock and not necessary for immediate plans.


BioBrick Promoter Measurements

- TOP10 cells were transformed with 2007 parts for BioBricks J63005 and J33202 (a constitutive yeast ADH1 promoter and a bacterial RBS+LacZ part), and 2008 parts for promoter constructs I20261 and I20267.

- The TOP10 cells transformed with J63005 and J33202 were added to an agarose plate with ampicilin, and those cells transformed with I20262 and I20267 were added to a plate with kanamycin.

- A sample from a glycerol stock for a death-resistant DB3.1 strain with the P1010-pSB3K3 plasmid was plated on a kanamycin plate, and a strain of DH5 alpha with a LacI mutation were added to a plate consisting of LB media wit no antibiotic.

- Glycerol stocks for TOP10 cells with promoter construction I20260, I20268, I20269, and I20270 were added to kanamycin plates.


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