Visit in US Embassy

Visas have been accorded to the whole team.

Preparation of alpha_linker under PT7 (BBa_K103019)

Michał K., Piotr

1. Clean-up of overnight digest reaction.
2. Digest of pSB1A3 carrying ΔA (BBa_K103003) with EcoRI and SacI (BamHI buffer), dephosphorylation with CIAP
3. Gel electrophoresis and gel-out of proper band - 2200 bp.
4. Ligation of digested pSB1A3 with alpha_linker under PT7 (BBa_K103019) fragment (1 hr).
5. Transformation of TOP10 with above ligation.
6. Tranformants plating on LB with ampicillin.

Preparation of omega_linker under PT7 (BBa_K103020)

Michał K., Piotr

1. Ligation of digested pSB2K3 vector from (30 September) with omega_linker under PT7 (BBa_K103020) fragment (1 hr).
2. Transformation of TOP10 with above ligation.
3. Tranformants plating on LB with kanamycin.

Preparation of AraC+pBAD+AID

Michał K., Piotr

1. Isolation of plasmid from culture inoculated on previous day - pMPMT5+AID without EcoRI site.
2. Control digest of isolated plasmids with EcoRI and BamHI (BamHI buffer) - proper clones found.
3. Temperature gradient PCR on pMPMT5+AID without EcoRI site plasmid using AraCl and AIDP_HindSpeNotPst primers (annealing temperature 40 - 60 °C; elongation length 2.30 min) to obtain AraC+pBAD+AID fragment. Gel electrophoresis.
4. PCR on pMPMT5+AID without EcoRI site plasmid using AraCl and AIDP_HindSpeNotPst primers (annealing temperature 45 °C; elongation length 2.30 min) to obtain AraC+pBAD+AID fragment.
5. Gel electrophoresis and gel-out of proper band 1800 bp.
6. Digest of isolated PCR product with XbaI and PstI (Tango buffer).
7. Clean-up of digested PCR product.

Preparation of pLac_OmpA_alpha

Michał K.

1. PCR on pACYC177+OmpA_omega_deltaA_alpha plasmid using AlphaL+Nde and AlphaP+link10+homo2 primers (annealing temperature 58 °C; elongation length 60s) to obtain alpha fragment.
2. Gel electrophoresis and gel-out of proper band 600 bp.