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Team:Newcastle/20 August 2010
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(New page: v=Subtilin Immunity= ==Aims== We have modified the promoters for Plasmid Vector (part 1), Promoter & RBS (part 2) and Double terminator (part 4), thus we aim to do Phusion PCR today. =...) |
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| + | =Transformation of ligated ''yneA'' into pGFPrrnB and pSB1C3= | ||
==Aims== | ==Aims== | ||
| - | + | To produce more colonies of the plasmid pGFPrrnB and pSB1C3 containing ''yneA'' with pGFPrrnB and pSB1C3 from[[Team:Newcastle/19_August_2010|yesterday]]. | |
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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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| - | + | {{Team:Newcastle/footer}} | |
Latest revision as of 00:33, 28 October 2010
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Transformation of ligated yneA into pGFPrrnB and pSB1C3
Aims
To produce more colonies of the plasmid pGFPrrnB and pSB1C3 containing yneA with pGFPrrnB and pSB1C3 fromyesterday.
Materials and Protocol
Please refer to transformation of E. coli.
   
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