Team:Warsaw/Calendar-Main/24 July 2008

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  1. Separate transformant colonies (tranformation of ligation of pACYC177+OmpA_alpha and omega_A from previous day) inoculated to liquid LB with kanamycin.

Antoni:

  1. Preparation of chemocompetent bacteria E. coli TOP10.

Cloning omega-A fusion on pKS (second attempt)

Michał L., Ewa, Marcin:

Sequencing confirms that we have obtained proper construct with omega-A fusion

Cloning of protein A DNA to OmpA constructs

  1. Colony PCR on colonies from plates with transformations pACYC177+OmpA_A_omega. Primers used: AL+SacI and AP+NotI
  2. Confirmed transformant colonies inoculated to liquid LB with kanamycin.
  3. Isolation of plasmids from cultures inocluated on previous day (pACYC177+OmpA_A_alpha).
  4. Control digest of isolated plasmids with BamHI and SacI.

Cloning of protein Z DNA to pET15b-OmpA-omega in place of OmpA
Paweł

  1. Ligations transformed into TOP10 and plated on LB + ampicillin.

Cloning omega-A fusion on pKS (second attempt)

Michał L., Ewa, Marcin:

  1. We have obtained white colonies of transformants and inoculated 10 of them on liquid LB+Amp100