PCR Amplification of DNA (KOD Polymerase)
From Bridges Lab Protocols
Materials
- Primers – order from IDT prediluted to 100 mM in TE. Make working solution of 1 uM (100x) in water with both sense and antisense primers combined (300uL water, 3uL of each primer)
- dNTPs – dilute to 2 mM each in water, make single use aliquots (50 uL aliquots... 10uL of each dNTP, 460uL water)
- Template – generally 1uL or less of a plasmid miniprep
- KOD Polymerase
Protocol
- Use the following volumes per reaction
- KOD Buffer #1, 5 uL of 10X buffer (Dave's Molecular Biology Stuff Box)
- Primers, 10uL of 1uM stock solution in water (both primers combined)
- dNTPs, 5uL of 2 mM (Dave's Molecular Biology Stuff Box)
- MgCl, 3uL of 3 mM (Dave's Molecular Biology Stuff Box)
- Sterile water, 28 uL
- Template 1 uL of a miniprep
- Polymerase 0.4 uL (KOD Polymerase found in "Enzymes" box in freezer)
- Run PCR Program (approx 3.5 to 4 hours). Normally use touchdown PCR (TD-KOD) as follows:
- 15s at 94
- 5s at 65
- 30s at 72
- 15s at 94
- 5s at 63 then -0.5/cycle
- 30s at 72
- Repeat steps 4-6 30 times
- 30s at 94
- 30s at 45
- 11 min at 72
- Hold at 4 until ready
- Purify PCR product if necessary using Qiagen kit (Add 5x PB)