Preparation of constructs with OmpA protein fusions and Cloning of protein Z DNA to OmpA constructs
1. Isolation of plasmids from cultures inocluated on previous day (pCACYC177 + OmpA_alpha and pACYC177+OmpA_Z_omega).
2. Control digestation of isolated plasmids with BamHI and SacI (we found good clones for both ligations).

Linked PCR Omega-A
reisolated PCR product PCR-omega - 4 µl
reisolated PCRT product A-homo - 13.5 µl
primer OmegaLS - 2 µl
primer APNot - 2 µl
Pfu buffer with Mg2+ - 5 µl
dNTPs - 1 µl
H2o - 22 µl
program:
1. 95°C - 3' 2. 95°C - 30" 3. 55°C - 45" 4. 68°C - 1' 5. go to step 2 25 x 6. 68° - 10' 7. keep in 4° gel electrophoresis