Team:Warsaw/Calendar-Main/11 July 2008

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<img src="https://static.igem.org/mediawiki/2008/9/9c/11_th_july.jpg" width=300 /><var>Fig. 1. Control BamHI and NotI digests  of plasmids, which were used in successful colony PCRs <b></b><br>
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1. Marker<br>
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2. slot 1. from yesterday's Omp_A_alpha colony PCR<br>
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2. slot 14. from yesterday's Omp_A_alpha colony PCR<br>
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2. slot 4. from yesterday's Omp_A_omega colony PCR<br>
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2. slot 10. from yesterday's Omp_A_omega colony PCR<br>

Revision as of 15:14, 25 October 2008

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Preparation of constructs with OmpA protein fusions

Michał K.

  1. Colony PCR with OmpaL_N and OmpaP_link primers on colonies from plates with transformations OmpA_alpha (annealing temperature - 55°C,45 s of elongation step).
  2. Gel electrophoresis.
  3. Confirmed transformant colonies inoculated to liquid LB with kanamycin.

Preparation of construct pKS with A protein

Michał L., Ewa, Marcin

  1. Colony PCR on colonies from plates with transformations pKS-A.
    Primers used: AL+SacI and AP+NotI
  2. Gel electrophoresis.
  3. Confirmed transformant colonies inoculated to liquid LB with ampicillin.

Cloning of protein Z DNA to pET15b-OmpA-alpha in place of OmpA

Piotr, Antoni

Isolation of plasmids from cultures inoculated on previous day.

Fig. 1. Control BamHI and NotI digests of plasmids, which were used in successful colony PCRs
1. Marker
2. slot 1. from yesterday's Omp_A_alpha colony PCR
2. slot 14. from yesterday's Omp_A_alpha colony PCR
2. slot 4. from yesterday's Omp_A_omega colony PCR
2. slot 10. from yesterday's Omp_A_omega colony PCR