Team:Warsaw/Calendar-Main/15 July 2008

From 2008.igem.org

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<h3> Preparation of alpha+A conctruct</h3><h4>Antoni</h4>
<h3> Preparation of alpha+A conctruct</h3><h4>Antoni</h4>
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<p><ol><li>Gradient PCR on alpha+A</li>
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<p><ol><li>Gradient PCR on alpha+A PCR products with <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL+SacI">AlphaL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AP+NotI">AP+NotI</a> primers.</li>
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<li>PCR with gradient of DMSO on alpha+A</li>
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<li>Gel electrophoresis. Again without satisfying results.
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<li>gel electrophoresis
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<li>Third PCR on alpha+A. This time two temperatures of annealing (68&deg;C and 72&deg;C) and gradient of DMSO</li>
 +
<li>Gel electrophoresis.
</li></ol></p>
</li></ol></p>

Revision as of 23:15, 24 October 2008

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Cloning of protein Z DNA to OmpA constructs

Michał K.

Two colonies (pACYC177+OmpA_Z_omega) was inoculated to liquid LB with kanamycin.

Preparation of alpha+A conctruct

Antoni

  1. Gradient PCR on alpha+A PCR products with AlphaL+SacI and AP+NotI primers.
  2. Gel electrophoresis. Again without satisfying results.
  3. Third PCR on alpha+A. This time two temperatures of annealing (68°C and 72°C) and gradient of DMSO
  4. Gel electrophoresis.

Polymerase Chain Ligation on linker-A and omega-linker

Michał L., Ewa, Marcin

  • reisolated PCR product omega-linker - 4 µl
  • reisolated PCR product linker-A - 13.5 µl
  • primer OmegaL+SacI - 2 µl
  • primer AP+NotI - 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 of products