Team:Warsaw/Calendar-Main/20 May 2008

From 2008.igem.org

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<li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> - translation fusion: AID + T7 RNA-polymerase - optimization (temperature gradient 60&deg;C - 80&deg;C).</p>
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<li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> - translation fusion: AID + T7 RNA-polymerase - optimization (annealing temperature gradient 60&deg;C - 80&deg;C).</p>
<p>Primers: </p>
<p>Primers: </p>
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Template DNA: purified PCR products from 16 May - AID and T7 RNA-polymerase for translation fusion <br>
Template DNA: purified PCR products from 16 May - AID and T7 RNA-polymerase for translation fusion <br>
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Elongation temperature: 73&deg;C<br>
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Annealing temperature: 73&deg;C<br>
Elongation time: 4 minutes <br>
Elongation time: 4 minutes <br>
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Revision as of 21:18, 1 October 2008

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Michał K:

  1. PCR - translation fusion: AID + T7 RNA-polymerase - optimization (annealing temperature gradient 60°C - 80°C).

    Primers:

    AIDlNrH and T7pXbSal
    Template DNA: purified PCR products from 16 May - AID and T7 RNA-polymerase for translation fusion
    Elongation time: 4 minutes
    35 cycles

  2. Optimization of PCR - translation fusion: AID + T7 RNA-polymerase - MgCl2 cocentration and number of cycles.

    Primers:

    AIDlNrH and T7pXbSal

    Template DNA: purified PCR products from 16 May - AID and T7 RNA-polymerase for translation fusion
    Annealing temperature: 73°C
    Elongation time: 4 minutes
  3. Gel electrophoresis of PCR products.

Michał L., Ewa, Marcin:

Plating colonies from the previous day on rifampicin