Product Description
Being a foremost firm, we are offering a top notch quality of Hot Start Taq DNA Polymerase PCR. It helps to eliminate the presence of undesired products due to non-specific DNA amplification. This solution is makes new strands of DNA. Hot Start Taq DNA Polymerase PCR is able to allow the reactions to be set up at room temperature. It is known for its high-amplification capacity as well as extreme specificity.
Exceptional Specificity and Robust PerformanceUtilizing hot start technology, this Taq DNA Polymerase PCR reagent delivers accurate and reproducible DNA amplification. The unique heat activation ensures minimal nonspecific amplification, making it ideal for high-demand research settings. Its resistance to common PCR inhibitors supports consistent results even in challenging samples.
Broad Application CompatibilityDesigned for versatility, this hot start Taq polymerase is suited for genotyping, sequencing, cloning, mutagenesis, and a wide selection of PCR-based research. Researchers can amplify fragment sizes ranging from 100 bp to 4 kb with reliable efficiency and yield.
Convenient and Reliable PackagingCatering to laboratories of all sizes, the product is available in 200, 500, and 1,000 reaction pack sizes. Properly sealed and shipped on dry ice, every batch retains optimal activity upon delivery. The solution is easy to use, whether you operate manually or with automated thermocyclers.
FAQ's of Hot Start Taq DNA Polymerase PCR:
Q: How should I store Hot Start Taq DNA Polymerase PCR for long-term stability?
A: For maximum stability and functionality, store the Hot Start Taq DNA Polymerase PCR at -20C. When stored under these conditions, the product maintains its activity for up to one year.
Q: What are the main benefits of using hot start technology in this PCR enzyme?
A: Hot start technology enhances specificity and greatly reduces nonspecific amplification. This leads to more accurate PCR results, particularly important for complex samples or when performing sensitive assays.
Q: When and how should the enzyme be activated during PCR setup?
A: The enzyme requires heat activation at 95C for 5 minutes at the beginning of the PCR protocol. This activation step ensures the polymerase remains inactive at lower temperatures, preventing unwanted amplification before thermal cycling.
Q: Where can this product be used and who are its intended users?
A: This polymerase is intended for research laboratory use in settings such as universities, biotechnology companies, or molecular biology research institutes. It is distributed, exported, and supplied from India.
Q: What processes and applications are compatible with this Hot Start Taq DNA Polymerase PCR?
A: The product is compatible with various molecular biology applications including genotyping, DNA sequencing, cloning, site-directed mutagenesis, and standard or real-time PCR amplification.
Q: How does this enzyme perform in the presence of common PCR inhibitors?
A: Hot Start Taq DNA Polymerase PCR is formulated to be resistant to common PCR inhibitors, ensuring optimal amplification even from difficult or partially purified DNA samples.
Q: What is the measurement and accuracy range for DNA amplification with this product?
A: This enzyme delivers high fidelity for PCR, reliably amplifying DNA fragments from 100 bp to 4 kb, making it suitable for a broad range of molecular biology applications.