Team:Warsaw/Calendar-Main/18 July 2008

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Cloning of protein A DNA to OmpA constructs

  1. Colony PCR on colonies from plates with transformations pACYC177+OmpA_A_omega and pACYC177+OmpA_A_alpha. Primers used: AL+SacI and AP+NotI
  2. Confirmed transformant colonies (found only on pACYC177+OmpA_A_alpha plate) inoculated to liquid LB with kanamycin.

Paweł: pET15b vector purified. Digest of pET15b and pACYClac+OmpA+omega with BamHI and NdeI
Gel-out of OmpA+omega (cutted from pACYClac+OmpA+omega, ~1350 bp)

Ligation of gel-outed fragment into digested pEt15b

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