Team:DTU-Denmark/Notebook/10 September 2013

From 2013.igem.org

(Difference between revisions)
(Colony PCR to verify Nir in pZA21::ara-tight)
Line 1: Line 1:
{{:Team:DTU-Denmark/Templates/StartPage|10 September}}
{{:Team:DTU-Denmark/Templates/StartPage|10 September}}
-
 
+
Navigate to the [[Team:DTU-Denmark/Notebook/9_September_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/11_September_2013|Next]] Entry
=lab 208=
=lab 208=
<hr/>
<hr/>

Revision as of 22:01, 16 September 2013

10 September

Navigate to the Previous or the Next Entry

Contents

lab 208


Main purpose


Who was in the lab


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

Navigate to the Previous or the Next Entry