Taqs like it hot and some like it hot from the start
Standard PCR or hot-start?
Standard Taq polymerase expresses optimal activity at 72°C but the enzyme becomes active from around 37°C. The low-temperature activity is substantial and has the disadvantage of permitting nonspecific amplification and mis-priming events during the initial lower-temperature phase of a PCR reaction. If your needs include automation of PCR, then consider using a hot-start Taq polymerase.
Hot-start polymerases, unlike standard Taq, are unreactive at ambient temperatures. Hot-start PCR techniques follow the same principles as conventional PCR, but enzymatic activity is suppressed until the first denaturation step has been accomplished. This minimizes nonspecific binding and mis-priming and results in improved specificity. In addition, the technology offers the significant convenience of reaction set up at room temperature making PCR automation possible. In some cases, even sensitivity is improved, because non-specific amplification depletes reaction components required for specific target amplification.
All Taq polymerases are suitable for:
Enzyme | Characteristics | Supplied with | |||||
---|---|---|---|---|---|---|---|
Hot-start (x min @ 95°C) |
Amplicon size | Extension rate | 5’-3’ exonuclease |
PCR buffer | Loading buffer | ||
P7250L Taq-B (Taq) |
Coming soon | ✘ No | <5 kb |
2–4 kb/min at 72°C |
✔ Yes | ✘ No | ✘ No |
P7620L TaqIT *(Stoffel) |
Coming soon | ✘ No | <7 kb | 2–4 kb/min at 72°C |
✘ No* | ✔ Yes | ✘ No |
201203 Taq |
✘ No | <7 kb | 2–4 kb/min at 72°C |
✔ Yes | ✔ Yes + Q‑Solution | ✔ Yes | |
201223 Taq PCR Core Kit |
✘ No | <7 kb |
2–4 kb/min at 72°C |
✔ Yes | ✔ Yes + dNTPs | ✔ Yes | |
203123 AllTaq PCR Core Kit |
✔ Yes (2 min.) | <9 kb | 1 min/kb at 68°C |
✔ Yes | ✔ Yes + dNTPs | ✔ Yes | |
203203 HotStarTaq |
✔ Yes (15 min.) | <7 kb | 2–4 kb/min at 72°C |
✔ Yes | ✔ Yes + Q‑Solution | ✘ No |
FAQs about enzymes for PCR and DNA amplification
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