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Team:Newcastle/20 August 2010
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==Materials and Protocol== | ==Materials and Protocol== | ||
| - | Please refer to [[Team:Newcastle/Gel_extraction|gel extraction]]. | + | Please refer to [[Team:Newcastle/Gel_extraction|gel extraction]] and [[TeamNewcastleNanoDrop_Spectrophotometer|nanodrop]]. |
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| + | ==Results== | ||
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| + | ==Discussion== | ||
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| + | ==Conclusion== | ||
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| + | =Transformation of Ligated Products= | ||
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| + | ==Aims== | ||
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| + | To produce more colonies of the ligated products of ''yneA'' with pGFPrrnB and pSB1C3. | ||
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| + | ==Materials and Protocol== | ||
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| + | Please refer to [[Team:Newcastle/Transformation_of_E._coli|transformation of E. coli]]. | ||
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Revision as of 11:07, 20 August 2010
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Contents |
Aims
Following yesterday's Phusion PCR, we plan to first perform gel electrophoresis, then gel extraction, and finally nanodrop to record the level of DNA.
Materials and protocol
Please refer to the gel electrophoresis, gel extraction and NanoDrop protocols. Vacuum manifold will be used.
Gel Extraction
Aims
To purify the PCR products of digested yneA, pGFPrrnB and pSB1C3 from yesterday.
Materials and Protocol
Please refer to gel extraction and nanodrop.
Results
Discussion
Conclusion
Transformation of Ligated Products
Aims
To produce more colonies of the ligated products of yneA with pGFPrrnB and pSB1C3.
Materials and Protocol
Please refer to transformation of E. coli.
   
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