From 2009.igem.org
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Revision as of 15:45, 17 October 2009
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Protocols
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PCR
(estimated time: 3 hours and 30 min)
- For every DNA sample you want to amplify, put:
- 2 µl buffer
- 0.6 µl MgCl2
- 0.4 µl dNTPs
- 1 µl DNA (or ddH2O for blank sample). If you are performing a colony PCR, pick up the desired colony from a plate with a tip and dip it in the solution.
- 0.2 µl Taq Polymerase
- 250 nM VF2 primer
- 250 nM VR primer
- A proper amount of ddH2O to have 20 µl of total reaction volume
- into an eppendorf tube.
- Put the eppendorf tube in the thermal cycler and set this program:
- 95°C 10 min
- CYCLE:
- 95°C 30 sec
- 60°C 1 min
- 72°C 1-3 min
- for 35 cycles
- 72°C 7 min
- 16°C forever.
- Now you can add a loading buffer to the solution and perform electrophoresis to check the amplified sequence length.
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MgCl2
Buffer
dNTPs
ddH2O
Taq Polymerase
VF2 primer
VR primer
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