Team:Warsaw/Calendar-Main/20 May 2008

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(Difference between revisions)
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<h4>Michał L., Ewa, Marcin:</h4>
<h4>Michał L., Ewa, Marcin:</h4>
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<p>Plating colonies from the previous day on rifampicin</p>
+
<p>1. Plating colonies from the previous day on rifampicin.</p>

Revision as of 21:21, 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:

1. Plating colonies from the previous day on rifampicin.