Team:Newcastle/13 August 2010
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==Results== | ==Results== | ||
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+ | The results from the Nanodrop Spectrophotometer of the four parts are as follows: | ||
+ | *'''Vector''' - 21.3 ng/μl | ||
+ | *'''Promoter''' - 28.8 ng/μl | ||
+ | *'''Coding sequence''' - 27.0 ng/μl | ||
+ | *'''Terminator''' - 27.5 ng/μl | ||
==Discussion== | ==Discussion== |
Revision as of 15:18, 13 August 2010
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Contents |
rocF BioBrick miniprep
rocF BioBrick nanodrop
rocF BioBrick gel electrophoresis
Expect band to be 3195bp.
Subtilin Immunity BioBrick
Aims
We plan to select three spaIFEG gene (part 3) PCR tubes, using Tms 51°C, 56°C and 61°C (we had confirmed it successful from yesterday's gel electrophoresis - please refer to the gel electrophoresis from yesterday). Gel extraction will then be performed, along with Plasmid Vector (part 1), Promoter & RBS (part 2) and Double terminator (part 4). Finally, NanoDrop will be performed on each of these four parts.
Materials and protocol
Please refer to the gel electrophoresis, gel extraction and NanoDrop protocols.
Results
The results from the Nanodrop Spectrophotometer of the four parts are as follows:
- Vector - 21.3 ng/μl
- Promoter - 28.8 ng/μl
- Coding sequence - 27.0 ng/μl
- Terminator - 27.5 ng/μl
Discussion
We chose the three spaIFEG gene (part 3) PCR tubes, using Tms 51°C, 56°C and 61°C because they were the mid-ranged Tms. Gel extraction was then performed, by firstly cutting the gels under U.V light, and then apply the protocol for completion.
Conclusion
The results from the NanoDrop reading suggests that our results were positive, which indicates that we have successfully extracted all the parts required for the Subtilin Immunity BioBrick. Gibson cloning method will be used next week.
Go back to our main Lab book page
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