Multiplex PCR refers to a PCR technology that simultaneously amplifies multiple gene loci in a single PCR reaction. The experiment processes are the same as conventional PCR, but multiple fragments can be detected simultaneously. It is of great significance in many fields such as scientific research and disease diagnosis, and is especially suitable for multi-site detection of trace samples. This kit contains Multiplex DNA Polymerase (multiplex PCR specific hot-start DNA polymerase), which has extremely high amplification specificity and sensitivity. Combined with 2 × Multiplex Buffer, a special buffer optimized for multiplex PCR reactions, this kit can stably and efficiently complete most multiplex PCR assays under default conditions. It has a wide range of applications and minimizes reaction system optimization steps.

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Taq Pro Multiplex DNA Polymerase is a new generation of hot-start DNA polymerase based on antibody modification and upgraded to improve template affinity. The High sensitivity version has been carefully optimized for multiplex PCR with strong amplification ability and high detection sensitivity. With the optimal buffer system for multiplex PCR, it is compatible with a wide range of product GC content and primer Tm values. The vast majority of multiplex PCR assays can be performed at a universal annealing temperature of 60°C without additional optimization.
This product has extremely high amplification efficiency, and can simultaneously amplify target fragments in the range of 50 – 3,500 bp; it has strong amplification ability, and can carry out enrichment of several hundred or more amplicons; excellent impurity tolerance, highly resistant to a variety of inhibitors and impurity types, and compatible with direct amplification of whole blood, blood cards, etc. The reagents have good stability, wide applicability, and are compatible with a variety of detection scenarios.

Vazyme oldal megtekintése (angol)

The post Taq Pro Multiplex DNA Polymerase (PM201) appeared first on SEQRS Kft..

Taq Pro Multiplex DNA Polymerase is a new generation of hot-start DNA polymerase based on antibody modification and upgraded to improve template affinity. The High specificity version has been carefully optimized for multiplex PCR with extremely high amplification specificity. With the optimal buffer system for multiplex PCR, it is compatible with a wide range of product GC content and primer Tm values, and most multiplex PCR assays can be completed at a universal annealing temperature of 60℃.
This product has extremely high amplification efficiency. All primers in the reaction system can be efficiently extended without additional optimization; the amplification preference is low, and the amplification efficiency is consistent for different types of primers and templates. Achieving high yields while maintaining good amplification uniformity; the amplification specificity is outstanding, which can effectively reduce the non-specific amplification caused by primer mismatch.

Vazyme oldal megtekintése (angol)

The post Taq Pro Multiplex DNA Polymerase (High specificity) (PM202) appeared first on SEQRS Kft..