Team:Warsaw/Calendar-Main/8 July 2008

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<table id="result">
<table id="result">
<tr><th>Product</th><th>Templates</th><th>Primers</th><th>Product length</th></tr>
<tr><th>Product</th><th>Templates</th><th>Primers</th><th>Product length</th></tr>
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<tr><th>Omega-A fusion</th><td>Omega-linker + linker-A</td><td>OmegaL+SacI + AP+NotI </td><td>900 bp</td></tr>
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<tr><th>Omega-A fusion</th><td>Omega-linker + linker-A</td><td><a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmegaL+SacI">OmegaL+SacI</a> + AP+NotI </td><td>900 bp</td></tr>
</table>
</table>
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Revision as of 17:04, 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 band (900 bp).
  3. PCL reaction to create omega-A fusion:

    ProductTemplatesPrimersProduct length
    Omega-A fusionOmega-linker + linker-AOmegaL+SacI + AP+NotI 900 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?).

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