Preparation of constructs with OmpA protein fusions

Michał K.

1. Isolation of pACYC177.
2. Digest of purified pACYC177 with NdeI and BamHI (Tango 2x buffer).
3. Gel electrophoresis (Fig. 2) and isolation of proper band (3200 bp).
4. Clean-up of OmpA_alpha and OmpA_omega digest products (Fig. 1).
5. Ligation of purified DNA (pACYC177 with OmpA_alpha and OmpA_omega DNA fragments).
6. Transformation of E.coli TOP10 with ligation products.
7. Plating transformants on LB+tetracycline.

Blue/white and rifampicin test

Michał L., Ewa, Marcin

Counting of blue colonies: