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Team:Newcastle/Colony PCR
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(New page: Colony PCR Materials to add accordingly: # 37.5µl of distilled H2O # 10µl of 5x GoTaq Buffer # Nucleotide DNTP # 2.5µl forward primer # 2.5µl backward primer # 1µl template DNA) |
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| - | + | {{Team:Newcastle/mainbanner}} | |
| - | + | =Colony PCR= | |
| - | # 37. | + | ==Materials required== |
| - | # | + | Add the following according: |
| + | |||
| + | # 37.5 µl of distilled H2O | ||
| + | # 10 µl of 5x GoTaq Buffer | ||
# Nucleotide DNTP | # Nucleotide DNTP | ||
| - | # 2. | + | # 2.5 µl forward primer |
| - | # 2. | + | # 2.5 µl backward primer |
| - | # | + | # 1 µl template DNA |
| + | |||
| + | ==Conditions for ThermoCycler:== | ||
| + | |||
| + | # Initialise - 95°C for 2 minutes. | ||
| + | # Denature - 95°C for 30 seconds. | ||
| + | # Anneal - 52°C for 30 seconds (melting temperature, Tm, of template) | ||
| + | # Extension - 75°C for 30 seconds | ||
| + | # Extension finish - 75°C for 5 minutes | ||
| + | # Hold - 4°C | ||
| + | |||
| + | Steps 2 to 4 are repeated for 30 cycles before continuing to step 5. | ||
| + | |||
| + | {{Team:Newcastle/footer}} | ||
Latest revision as of 14:52, 28 July 2010
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Colony PCR
Materials required
Add the following according:
- 37.5 µl of distilled H2O
- 10 µl of 5x GoTaq Buffer
- Nucleotide DNTP
- 2.5 µl forward primer
- 2.5 µl backward primer
- 1 µl template DNA
Conditions for ThermoCycler:
- Initialise - 95°C for 2 minutes.
- Denature - 95°C for 30 seconds.
- Anneal - 52°C for 30 seconds (melting temperature, Tm, of template)
- Extension - 75°C for 30 seconds
- Extension finish - 75°C for 5 minutes
- Hold - 4°C
Steps 2 to 4 are repeated for 30 cycles before continuing to step 5.
   
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