Cloning of protein A DNA to OmpA constructs

1. Digest of pKS-A plasmid, pACYC177+OmpA_omega and pACYC177+OmpA_alpha with NotI and SacI (pACYC177 were also dephosporylated with CIAP)
2. Gel electrophoresis and gel-out of proper bands (420 bp - pKS-A lane, 4050 bp - pACYC177+OmpA_omega lane and 4300 bp pACYC177+OmpA_alpha lane).
3. Ligation of A DNA fragment with both pACYC177 vectors.
4. Transformation of E. coli TOP10 strain with ligations.
5. Transformants plating on LB + kanamycin.

Paweł

1. Digest of pET15b-OmpA-omega and Z(in GeneArt vector) with NdeI and NotI.
2. Gel-out of Z (~200 bp band).
3. Ligation of Z into digested pET15b-OmpA-omega.

Cloning of protein A DNA to pET15b+OmpA-alfa plasmid in place of OmpA
Antoni

1. Colony PCR on colonies from plates with transformations pGeneart+A Primers used: AP_Not and AL_Sac
2. Confirmed transformant colonies inoculated to liquid LB with ampicillin
3. Inoculated to liquid LB with ampicillin pET15b+OmpA-alfa