Team:Warsaw/Calendar-Main/1 July 2008

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Change of the reporter from pZC320 with B-galactosidase to GFP or RFP

Piotr, Weronika

  1. Isolation of plasmids from transformants.
  2. Control digest of plasmids with NotI.
  3. Gel electrophoresis of digested DNA - there where no proper plasmids
  4. Isolation of pZC320
  5. Isolation of pSB1A2 standard plasmids carrying parts: BBa_E0840(GFP genetrator) and BBa_J04450 (RFP generator)
  6. Overnight digest of pSB1A2 standard plasmids carrying parts: BBa_E0840(GFP genetrator) and BBa_J04450 (RFP generator) with NotI
  7. Overnight digest of pZC320 with NotI and dephosphorylation with CIAP

Cloning alpha-A and omega-A fusions on pKS

Michał L., Ewa, Marcin

  1. Isolation of plasmids from transformants.
  2. Control digest of plasmids with SacI+NotI (BamHI buffer).
  3. Gel electrophoresis of digested DNA.

We have successfully cloned A-alpha and A-omega fusions on pKS vector. The DNA will be now sequenced to ensure that our constructs are correct.

Preparation of constructs on pET15b: OmpA_alpha and OmpA_omega

Paweł

  1. Isolation of pET15b plasmid.
  2. Overnight digest of pET15b plasmid with NdeI and BamHI (Tango 2x buffer), dephosphorylation with CIAP.