PCM14, Multiplex Pro MasterMix
Multiplex Pro MasterMix
2024-11-04
Multiplex bisDNA probe Mixture
2024-11-04
Show all

FastStar DNA Polymerase

Datasheet | MSDS | COA | Blog | Request

PC16, FastStar DNA Polymerase

Manual

Product Number: PC16

Shipping and Storage

-20°C.

Components

ComponentPC16 500UPC16 5KUPC16 50KU
FastStar DNA Polymerase (5 U/μL)100μL1ml10ml

Description

FastStar DNA Polymerase is a mixture of anti Taq enzyme monoclonal antibodies and Taq DNA Polymerase suitable for Hot Start PCR.When using Taq enzyme antibodies for PCR amplification, the binding of Taq enzyme antibodies to Taq enzyme inhibits DNA polymerase activity before high-temperature denaturation, which can effectively inhibit non-specific annealing of primers and non-specific amplification caused by primer dimers under low temperature conditions.Taq enzyme antibodies undergo denaturation in the initial DNA denaturation step of PCR reaction, and polymerase activity is restored, achieving a hot start effect. This product does not require special inactivation of Taq enzyme antibodies and can be used under conventional PCR reaction conditions.

FastStar DNA Polymerase has 5'→3' DNA polymerase activity and 5'-3' exonase activity, without 3'-5' exonase activity. The enzyme has an elongation rate of 2kb/min and can amplify fragments up to 5kb in length.The amplified PCR product has an "A" base attached to its 3'end, making it suitable for direct T/A cloning. The blocking rate of polymerase activity reaches over 95% at temperatures of 55℃ and below. Heating at 95℃ for 5 seconds can restore DNA polymerase activity.This product has the characteristics of fast extension speed and high amplification efficiency, and is mainly suitable for experiments such as PCR amplification of DNA fragments and DNA sequence determination.

Unit definition

Using activated salmon sperm DNA as a template/primer, the amount of enzyme required to incorporate 10nmol of deoxynucleotides into acidic insoluble substances is defined as 1 active unit (U) at 74°C for 30 minutes.

Quality Control

After multiple column purification, the purity was detected by SDS-PAGE to be over 99%;no exogenous nuclease activity was detected,Closed at 55℃ for 30 minutes without polymerase activity;95℃ for 5 seconds, fully activated.

PC16, FastStar DNA Polymerase

Get a quote now







    Mail