Team:Newcastle/PCR

From 2010.igem.org

(Difference between revisions)
Line 5: Line 5:
===Materials to add accordingly===
===Materials to add accordingly===
-
# 37.5 µl of distilled H2O
+
# 37.5 µl of distilled H<sub>2</sub>O
# 10 µl of 5x GoTaq Buffer
# 10 µl of 5x GoTaq Buffer
# 1 µl of nucleotide DNTP
# 1 µl of nucleotide DNTP
Line 27: Line 27:
===Materials to add accordingly===
===Materials to add accordingly===
-
# 27.5 µl of distilled H2O
+
# 27.5 µl of distilled H<sub>2</sub>O
# 10 µl of 5x Buffer
# 10 µl of 5x Buffer
# 1 µl of nucleotide DNTP
# 1 µl of nucleotide DNTP

Revision as of 14:09, 27 July 2010

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Contents

GoTaq PCR

Materials to add accordingly

  1. 37.5 µl of distilled H2O
  2. 10 µl of 5x GoTaq Buffer
  3. 1 µl of nucleotide DNTP
  4. 2.5 µl forward primer
  5. 2.5 µl backward primer
  6. 1 µl template DNA

Conditions for ThermoCycler

  1. Initialise - 95°C for 2 minutes.
  2. Denature - 95°C for 30 seconds.
  3. Anneal - 52°C for 30 seconds (melting temperature, Tm, of template)
  4. Extension - 75°C for 30 seconds
  5. Extension finish - 75°C for 5 minutes
  6. Hold - 4°C

Steps 2 to 4 are repeated for 30 cycles before continuing to step 5.

Phusion PCR

Materials to add accordingly

  1. 27.5 µl of distilled H2O
  2. 10 µl of 5x Buffer
  3. 1 µl of nucleotide DNTP
  4. 5 µl forward primer
  5. 5 µl backward primer
  6. 1 µl template DNA
  7. 0.5 µl of Fusion

Conditions for ThermoCycler

  1. Initialise - 98°C for 30 seconds.
  2. Denature - 98°C for 10 seconds.
  3. Anneal - x°C for 20 seconds (melting temperature, Tm, of template)
  4. Extension - 72°C for 30 seconds per kb
  5. Extension finish - 72°C for 5-10 minutes
  6. Hold - 4°C

Steps 2 to 4 are repeated for 30 cycles before continuing to step 5.

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