Team:DTU-Denmark/Notebook/10 September 2013

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=lab 208=
=lab 208=
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==Main purpose==
 
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==Who was in the lab==
==Who was in the lab==
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Kristian, Henrike
==Procedure==
==Procedure==

Latest revision as of 12:13, 4 October 2013

10 September

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Contents

lab 208


Who was in the lab


Kristian, Henrike

Procedure


Colony PCR to verify Nir in pZA21::ara-tight

Redid colony PCR with sequencing primers instead. Two primer pairs to test for the two USER parts. Pair 1: Nir_FW_4_Seq + Nir_RV_5_Seq . Pair 2: Nir_FW_13_Seq + Nir_RV_14_Seq.

Used Q5 premix. Calculated annealing temperature for pair 1: 60C, pair 2: 64C

Note: The resulting gel showed a lot of bands that are consistent for all colonies. We repeated the PCR on the next day for one of the colonies with the following annealing temperatures: pair 1: 67C, pair 2: 68C

Results


Gel

  • 1 kb ladder
  • Nir colony 1, primer pair 1
  • Nir colony 1, primer pair 2
  • Nir colony 2, primer pair 1
  • Nir colony 2, primer pair 2
  • Nir colony 3, primer pair 1
  • Nir colony 3, primer pair 2
  • Nir colony 4, primer pair 1
  • Nir colony 5, primer pair 2
  • Nir colony 5, primer pair 1
  • Nir colony 5, primer pair 2
  • Nir colony 6, primer pair 1
  • Nir colony 6, primer pair 2
  • 1 kb ladder

Colony pcr 10. sep..jpg

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