From 2010.igem.org
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Latest revision as of 09:43, 17 August 2010
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PCR with Pfu Polymerase
Source: Promega Usage Information for the Pfu Polymerase
In a sterile, nuclease free PCR-tube mix following components:
Component
| Volume
| Final concentration
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Pfu DNA Polymerase 10x Buffer (with MgSO4)
| 5 µl
| 1x
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dNTP 10mM each
| 1µl
| 200µM each
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upstream primer
| 5-50pmol (from 100pmol/µl e.g. 2,5µl)
| 0,1- 1 µM
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downstream primer
| 5-50pmol (from 100pmol/µl e.g. 2,5µl)
| 0,1- 1 µM
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DNA Template
| variable (dependent on DNA conc.)
| <0,5µg/50µl (e.g. 0,3)
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Pfu DNA Polymerase (3u/µl)
| 0,5µl
| ~1,25u/50µl
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nuclease free water to final volume of
| 50 µl
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Recommended thermal cycling conditions for Pfu Polymerase:
Step
| Temperature
| Time
| Number of Cycles
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Initial Denaturation
| 95°C
| 1-2min
| 1
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Denaturation
| 95°C
| 0,5-1min
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Annealing
| 42-65°C (dependent on primer and template)
| 30sec
| 25-35
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Extension
| 72-74°C
| 2-4min (2min/kb)
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Final Extension
| 72-74°C
| 5 min
| 1
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Soak (end)
| 4°C (on our thermalcyclers 12°C)
| Indefinite
| 1
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