Team:Warsaw/Calendar-Main/16 June 2008

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<h4>Michał L., Ewa, Marcin:</h4>
 
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<li>Colony <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a><br>
 
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Template: DNA isolated from white colonies<br>
 
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Primers: <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqR">pZCseqR</a><br>
 
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Annealing time:<br>
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<h3>Preparation of constructs with OmpA protein fusions<br>
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Michał K.</h3>
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Number of cycles:</li>
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<li>DNA gel electrophoresis of PCR products.</li>
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<li>Gel-out of proper products (~1200 bp).</li>
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<li>Sequencing of proper fragments using primer <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a>.</li></ol>
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<h3>Preparation of constructs with OmpA protein fusions</h3>
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<h4>Michał K.:</h4>
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<li>Electrophoresis to estimate the concentration of isolated DNA.</li>
<li>Electrophoresis to estimate the concentration of isolated DNA.</li>
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<h4>Michał L., Ewa, Marcin:</h4>
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<ol>
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<li>Colony <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a><br>
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Template: DNA isolated from white colonies<br>
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Primers: <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqR">pZCseqR</a><br>
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Annealing time: <br>
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Number of cycles: </li>
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<li>DNA gel electrophoresis of PCR products.</li>
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<li>Gel-out of proper products (~1200 bp).</li>
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<li>Sequencing of proper fragments using primer <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a>.</li></ol>
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Revision as of 15:09, 9 October 2008

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Preparation of constructs with OmpA protein fusions
Michał K.

  1. PCR on pB30D plasmid with OmpaL_N and OmpaP_link primers (15 cycles, elongation duration 45 s, annealing temperature 63°C).
  2. PCR on pUC19 plasmid with AlphaL_link and AlphaP_XB primers (20 cycles, elongation duration 45 s, annealing temperature 63°C).
  3. PCR on pUC19 plasmid with OmegaL_link and OmegaP_EPB primers (20 cycles, elongation duration 30 s, annealing temperature 58°C).
    As a result we got three PCR products: OmpA_linker and two fragments of TEM1 beta-lactamese: linker_alpha and linker_omega.
  4. Gel electrophoresis of PCR products and gel-out of proper bands (OmpA_linker - 500 bp, linker_alpha - 600 bp and linker_omega - 350 bp).
  5. Electrophoresis to estimate the concentration of isolated DNA.

Michał L., Ewa, Marcin:

  1. Colony PCR
    Template: DNA isolated from white colonies
    Primers: pZCseqL and pZCseqR
    Annealing time:
    Number of cycles:
  2. DNA gel electrophoresis of PCR products.
  3. Gel-out of proper products (~1200 bp).
  4. Sequencing of proper fragments using primer pZCseqL.