User:Stuart McKellar/Notebook/Bird Sex Testing/2012/12/01

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(Entry title)
Current revision (01:31, 1 December 2012) (view source)
(higher annealing temp)
 
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total volume in each is 25μL.
total volume in each is 25μL.
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PCR: 94°C for 2m30s, 35 cycles of: 95°C 30s, 65°C for 30s, 72°C for 30s; final elongation 72°C for 5 mins.
+
PCR: 94°C for 2m30s, 35 cycles of: 95°C 30s, 65°C for 30s, 72°C for 30s; final elongation 72°C for 5 mins( actually went 10 mins by accident).
results to be determined via agar gel electrophoresis on 1% gel stained using gelgreen.
results to be determined via agar gel electrophoresis on 1% gel stained using gelgreen.

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higher annealing temp

Aim: test the p2/p8 and 2550/2178 primers at 65°C.

Method:

Sample 1:

  • A6: p2/p8 primers
  • B6: 2550/2178 primers

Sample 2:

  • C6: p2/p8 primers
  • D6: 2550/2178 primers

Negative control - no DNA (1ul h2O, 2550/2178 primers.)

Master mix (5x):

  • 12.5μL buffer 10x
  • 12.5μL dNTPS
  • 7.5μL MgCl2
  • 62.5 H2O
  • 1μL Taq


  • A6: p2/p8 primers (2.5μL each, 1μL DNA) + 18.5 Master Mix
  • B6: 2550/2178 primers (2.5μL each, 1μL DNA) + 18.5 Master Mix
  • C6: p2/p8 primers (2.5μL each, 1μL DNA) + 18.5 Master Mix
  • D6: 2550/2178 primers (2.5μL each, 1μL DNA) + 18.5 Master Mix

total volume in each is 25μL.

PCR: 94°C for 2m30s, 35 cycles of: 95°C 30s, 65°C for 30s, 72°C for 30s; final elongation 72°C for 5 mins( actually went 10 mins by accident).

results to be determined via agar gel electrophoresis on 1% gel stained using gelgreen.



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