Team:Newcastle/20 August 2010

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{{Team:Newcastle/mainbanner}}
{{Team:Newcastle/mainbanner}}
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=Aims=
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=Transformation of ligated ''yneA'' into pGFPrrnB and pSB1C3=
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Following yesterday's Phusion PCR, we plan to first perform gel electrophoresis, then gel extraction, and finally nanodrop to record the level of DNA.
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==Materials and protocol==
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Please refer to the [[Team:Newcastle/Gel_electrophoresis| gel electrophoresis]], [[Team:Newcastle/Gel_extraction| gel extraction]] and [[TeamNewcastleNanoDrop_Spectrophotometer| NanoDrop]] protocols. '''Vacuum manifold''' will be used.
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=Gel Extraction=
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==Aims==
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To purify the PCR products of digested ''yneA'', 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/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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=Miniprep of ''yneA'', pGFPrrnB and pSB1C3=
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==Aim==
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To produce stocks of ''yneA'', pGFPrrnB and pSB1C3.
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==Materials and Protocol==
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Please refer to [[Team:Newcastle/Qiagen_Minipreps|miniprep]] 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==
==Aims==
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To produce more colonies of the ligated products of ''yneA'' with pGFPrrnB and pSB1C3.
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To produce more colonies of the plasmid pGFPrrnB and pSB1C3 containing ''yneA'' with pGFPrrnB and pSB1C3 from[[Team:Newcastle/19_August_2010|yesterday]].
==Materials and Protocol==
==Materials and Protocol==
Please refer to [[Team:Newcastle/Transformation_of_E._coli|transformation of E. coli]].
Please refer to [[Team:Newcastle/Transformation_of_E._coli|transformation of E. coli]].
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=Ligation of ''yneA'' with Vectors=
 
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==Aims==
 
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To ligate ''yneA'' with pGFPrrnB and ''yneA'' with pSB1C3.
 
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==Materials and Protocol==
 
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Please refer to [[Team:Newcastle/Ligation|ligation]].
 
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==Results, Discussion and Conclusion==
 
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Please refer to [[Team:Newcastle/23_August_2010|23.08.10]].
 
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{{Team:Newcastle/footer}}
{{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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