Team:Warsaw/Calendar-Main/20 May 2008

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3.  Gel electrophoresis of PCR products.
3.  Gel electrophoresis of PCR products.
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Michał L., Ewa, Marcin:
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Plating colonies from the previous day on rifampicin

Revision as of 16:08, 1 October 2008

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Michał K:
1.PCR - translation fusion: AID + T7 RNA-polymerase - optimalization (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. Optimalization 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

Elongation temperature: 73°C
Annealing time: 4 minutes

3. Gel electrophoresis of PCR products.

Michał L., Ewa, Marcin:

Plating colonies from the previous day on rifampicin