| Fidelity (vs. Taq) | 1X |
|---|---|
| Hot Start | No |
| Overhang | 3'-A |
| Polymerase | <i>Taq</i> DNA Polymerase |
| Product Type | <i>Taq</i> DNA Polymerase (Recombinant) |
| Quantity | 500 Units |
| Reaction Format | Separate Components |
| Shipping Condition | Dry Ice |
| Concentration | 5 U/μL |
| For Use With (Application) | Standard PCR |
| GC-Rich PCR Performance | Low |
| Reaction Speed | Standard |
| Unit Size | Each |
Answer:This configuration contains 500 units at 5 U/µL.
Answer:No. It has no detectable 3′→5′ proofreading exonuclease activity.
Answer:It is intended for routine DNA amplification where standard Taq performance is appropriate.
Recombinant Taq DNA Polymerase is a thermostable enzyme for routine PCR amplification of DNA templates. This configuration provides 500 units at 5 U/µL. The enzyme catalyzes 5′→3′ DNA synthesis and has no detectable 3′→5′ proofreading exonuclease activity, so it is appropriate for standard amplification workflows where high proofreading fidelity is not required. Taq also has low 5′→3′ exonuclease activity and commonly adds a single extra adenine to the 3′ ends of PCR products, which can be useful for TA cloning. The enzyme is supplied with reaction buffer for conventional PCR setup and is suitable for amplification from genomic, plasmid, and cDNA templates when primers and cycling conditions are optimized for the target. Use an appropriate magnesium concentration and extension time based on amplicon length, template complexity, and downstream application.
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