Team:Warsaw/Calendar-Main/8 July 2008

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<h3>Preparation of construct pKS with A protein<br>
<h3>Preparation of construct pKS with A protein<br>
Michał L., Marcin:</h3>
Michał L., Marcin:</h3>

Revision as of 14:13, 11 October 2008

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Preparation of constructs with OmpA protein fusions
Piotr

  1. Transformation of E. coli TOP10 strain with ligation from previous day.
  2. Transformants plating on LB + kanamycin.


Cloning omega-A fusion on pKS (second attempt)

Michał L., Ewa, Marcin:

  1. Gel electrophoresis of PCR products
  2. Gel-out of proper bands
  3. PCL reaction to create omega-A fusion:

    ProductTemplatesPrimersProduct length
    Omega-A fusionOmega-linker + linker-AOmegaL+SacI + AP+NotI 1440 bp

    PCL program for omega-A fusion
    TemperatureTime
    94°C4:00
    94°C0:3028 cycles
    48°C-58°C0:45
    68°C2:00
    68°C10:00
    4°Cinfinite

  4. Gel electrophoresis of PCL products
  5. We have obtained no PCL product (weird?)

Preparation of construct pKS with A protein
Michał L., Marcin:

  1. Inactivation of digestion enzymes and CIAP.
  2. Ligation of digested PCR product and pKS 2h at room temperature.
  3. Transformation of E. coli TOP10 strain with 7 µl of ligation mix.
  4. Transformants plating on LB + ampicillin + X-gal + IPTG.