Team:Newcastle/4 August 2010
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==Aim== | ==Aim== | ||
- | The aim of this experiment is to amplify 6 different RocF fragments for the construction of [[Team:Newcastle/Urease|''rocF'' BioBrick]] using | + | The aim of this experiment is to amplify 6 different RocF fragments for the construction of [[Team:Newcastle/Urease|''rocF'' BioBrick]] using Phusion PCR . |
==Materials and Protocol== | ==Materials and Protocol== | ||
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!'''Tube''' | !'''Tube''' | ||
!'''Part to be amplified''' | !'''Part to be amplified''' | ||
- | !'''DNA | + | !'''Template DNA''' |
!'''Forward primer''' | !'''Forward primer''' | ||
!'''Reverse Primer''' | !'''Reverse Primer''' |
Revision as of 22:44, 27 October 2010
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Contents |
Cloning the rocF BioBrick
Aim
The aim of this experiment is to amplify 6 different RocF fragments for the construction of rocF BioBrick using Phusion PCR .
Materials and Protocol
Please refer to PCR for Phusion PCR protocol. The details for the 6 PCR reactions are mentioned below:
Phusion PCR
Tube | Part to be amplified | Template DNA | Forward primer | Reverse Primer | Melting Temperature (Tm in °C) | Size of the fragment (in bp) | Extension time* (in seconds) |
---|---|---|---|---|---|---|---|
1 | Plasmid Vector | pSB1C3 | P1V1 forward | P2V1 reverse | 58 | 2072 approx. | 60 |
2 | Pspacoid Promoter | pMutin4 | P1P1 forward | P2P1 reverse | 49 | 106 approx. | 15 |
3 | 1st fragment of rocF CDS | B. subtilis 168 chromosome | P1S1 forward | P2S1 reverse | 58 | 246 approx. | 15 |
4 | 2nd fragment of rocF CDS | B. subtilis 168 chromosome | P3S2 forward | P4S2 reverse | 65 | 597 approx. | 20 |
5 | 3rd fragment of rocF CDS | B. subtilis 168 chromosome | P5S3 forward | P6S3 reverse | 66 | 125 approx. | 15 |
6 | Double Terminator | pSB1AK3 consisting BBa_B0014 biobrick | P1T1 forward | P2T1 reverse | 56 | 116 approx. | 15 |
Table 1: Table represents 6 different Phusion PCR reactions and the parts which are amplified so that they can be ligated together with the help of Gibson Cloning method.
- The extension rate of the Phusion polymerase is at 1Kb/ 30 seconds. Therefore the extension time of each PCR reaction is different.
- To learn more about the rocF fragments, please refer to the Cloning strategy for rocF.
Discussion
The 6 Phusion PCR reactions were done. However gel electrophoresis was not done to check for the fragments.
Conclusion
Gel electrophoresis will be done tomorrow, 5th August, 2010 to confirm that the RocF fragments have been amplified.
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