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Team:Newcastle/26 July 2010
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Revision as of 19:57, 26 July 2010 by Swoodhouse (Talk | contribs)
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Preparation for cloning of the rocF BioBrick
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A
- Re-hydrated pSB1C3 (the plasmid we will be submitting our BioBricks to the registry in) and pSB1AK3 with BBa_B0014 (the double terminator we will be using for the rocF BioBrick) from the parts distribution.
- Transformed and plated separate .. of E. coli DH5α with the above two plasmids, with BBa_K143062 (LacI BioBrick sent to us by Imperial, we will using this to help us characterise many of our BioBricks, including rocF) and with a control which we had prepared from our training week - pSB1AT3 with rfp insert.
Overnight cultures of B. subtilis 168 for chromosomal DNA extraction
The rocF coding sequence is to be taken from B. subtilis 168 chromosomal DNA by PCR. Before we can do this we need to extract 168 chromosomal DNA.
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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