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Team:Newcastle/26 July 2010
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===Colony PCR of Genomic DNA=== | ===Colony PCR of Genomic DNA=== | ||
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Please refer to Lab book dated 27.7.2010. | Please refer to Lab book dated 27.7.2010. | ||
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Revision as of 19:03, 26 July 2010
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Contents |
Colony PCR of Genomic DNA
Aim:
To determine whether the genes have been inserted into the plasmid of B. Subtilis 168.
Materials:
- Pipette
- Microfuge
- Microtubes
- Distilled H2O
- Nucleotide DNTP
- 5x GoTaq buffer
- Template DNA (B. Subtilis ATCC 6633, 1:1 and 1:2)
- Forward and reverse primers
Protocol:
- For the full protocol, please refer to Colony PCR in Protocol List.
Conditions in ThermoCycler:
- Melting temperature, Tm used for Anneal step is 59°C.
Results:
Gel electrophoresis will be run tomorrow to determine the results.
Conclusion:
Please refer to Lab book dated 27.7.2010.
   
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