Team:DTU-Denmark/Notebook/25 August 2013

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==Main purpose==
==Main purpose==
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*PCR
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*colony PCR
==Who was in the lab==
==Who was in the lab==

Revision as of 17:59, 28 September 2013

25 August 2013

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Contents

Lab 208


Main purpose


  • colony PCR

Who was in the lab


Procedure


Colony PCR

Performed colony PCR to confirm insert for HAO, AMO, cycAX and Nir transformants. Used Q5 premix with the following reaction mix:

compound amount
Q5 mix 25 uL
FW primer 3 uL
RV primer 3 uL
template 1 uL
MilliQ 18 uL

Template was made by resuspending 1 culture in 100uL MilliQ.

program:

temperature time cycles
98C 10:00 -
98C 0:10 36
annealing temperature 0:30 36
72C 0:20 36
72C 5:00 -
10C hold -

details (primers, temp, expected fragment length):

  • cycAX - FW_1, RV_2, 61C, 749bp
  • HAO - FW_2, RV_3, 64C, 751bp
  • AMO - FW_2, RV_3, 63C, 750bp
  • Nir - FW_2, RV_3, 64C, 733bp
  • Nir - FW_5, RV_6, 71C, 737bp

Results


Conclusion


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