Team:Tuebingen/Notebook/Protocols/pcr
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PCR
Reagents
39.5 µL | Aqua dest. |
2.5 µL | dNTPs (200 µM each) |
1 µL | DNA (c = 100 ng/µL) |
5.0 µL | Taq-Buffer |
0.5 µL | Forward primer |
0.5 µL | Reverse primer |
1 µL | Taq/Pfu polymerases (9+1) |
Procedure
Mix all reagents in the given order (Important: add polymerases last!) and transfer in one 0.2 mL Eppendorf-tube ("PCR-tube"). Run cycler according to your requirements.
This protocol yields exactly one single reaction mixture! Scale linearly for multiple reaction mixtures and keep mixture on ice or even better at -20 °C for best results.
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