Basic information
Date:
Wed, 2008-03-26 00:00
Gene:
Template:
dna
Procedure
PCR cocktail:
Component | Volume (ul) | Mix (ul) |
Forward primer | ||
Reversed primer | ||
Buffer | ||
MgCl2 | ||
dNTPs | ||
Taq | ||
DNA (if nested) | ||
ddH2O |
||
Total volume |
Forward primer(s):
Thermal cycling (abbreviated):
95ºC@4min, 1x(94ºC@30sec, 55-51ºC@30sec,72ºC@30), 35x(94ºC@30sec, 50ºC@30sec, 72ºC@60sec),72ºC@10min
PCR machine:
GeneAmp
Thermal cycling:
Step | Comment | Cycles | Time (sec) | Temperature (°C) |
Initialization | For DNA polymerases that need hot-start heat activation | 1 | ||
Denaturation | DNA melting producing single-stranded DNA | 1 | 240 | 95 |
Amplification | 1 | - | - | |
Denaturation | DNA melting producing single-stranded DNA |
- | 30 | 94 |
Annealing | The primer binds to the template | - | 30 | 55-51 |
Extension | The DNA polymerase synthesizes new DNA | - | 30 | 72 |
Amplification | 35 | |||
Denaturation | 30 | 94 | ||
Annealing | 30 | 50 | ||
Extension | 60 | 72 | ||
Final elongation | Any remaining single-stranded DNA is extended | 600 | 72 | |
Final hold | Short-term storage | 1 | - | 12 |
Notes:
Negativa PCR reampades med 28Spart1F/28Spart1R enligt bifogade PCR bild.
Reversed primer(s):
File attachments:
People:
Products and Equipment:
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