Taq polymerase enzymes are the cornerstone of PCR workflows, providing fast and reliable DNA amplification. Known for their heat stability, hot-start Taq DNA polymerases are ideal for reducing nonspecific amplification and increasing assay sensitivity in PCR reactions. These enzymes enable rapid and efficient DNA synthesis, making them suitable for both routine and high-throughput applications. Whether you need a PCR-ready Taq polymerase or a specialized Taq polymerase for challenging samples, our products ensure accurate and reproducible results.
Hot-start PCR options, including antibody- and chemically mediated methods, enhance specificity and enable room-temperature setup. Antibody-mediated hot-start Taq uses a thermostable antibody to block activity until thermal cycling, preventing nonspecific amplification. Chemically mediated hot-start Taq relies on a heat-activated modification for precise control. Both methods improve specificity, making them ideal for complex templates and low-copy targets.
Designed to optimize speed and performance, Taq DNA Polymerases from QIAGEN PCR offers exceptional reliability for various molecular biology workflows. With advanced formulations to reduce error rates and improve amplification efficiency, our low-error Taq polymerases for PCR empower researchers to achieve precise, high-quality results, even under demanding conditions.
If you are looking for polymerases other than Taq, go to High-Fidelity DNA Polymerases for Molecular Research