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                    Products > High Specificity PCR > HS Taq DNA Polymerase(P1081/P1082/P1083/P1084)

                    HS Taq DNA Polymerase(P1081/P1082/P1083/P1084)


                    ? HSTM Taq DNA Polymerase has two concentrations with 2.5 U/μl and 5 U/μl, default package is 5 U/μl.
                    ? 10×HSTM PCR Buffer (Mg2+ Plus) can replace with 10×PCR Buffer (Mg2+ free) and 25 mM MgCl2. Please choose the appropriate package for your experiment.

                    HSTM Taq DNA Polymerase is a thermostable recombinant DNA polymerase derived from thermophilic bacterium Thermus aquaticus , its molecular weight is 94 kDa. HSTM Taq DNA Polymerase can amplify DNA target up to 5 kb. The elongation velocity is 0.9~1.2kb/min. It has 5' to 3' polymerase activity but lacks of 3' to 5' exoneclease activity, which results in a 3'-dA overhangs PCR product. All conponents of the HSTM PCR Buffer are at optimal concentration for efficient amplification, it contributes to highly specific incorporation of primer and template.

                    Highly thermostable -have a half-life of over 40 min at  95°C incubation
                    Generates 3'-dA overhangs PCR products

                    Routine PCR
                    PCR labeling
                    PCR sequencing
                    Generate PCR product for TA cloning

                    Quality Control 
                    The absence of endodeoxyribonucleases, exodeoxyribonucleases and ribonucleases confirmed by appropriate quality tests

                    Functionally tested in PCR

                    10x HSTM PCR Buffer with Mg2+

                    200 mM Tris-Cl(PH 8.8), 100 mM KCl, 16 mM MgSO4, 1% Triton-X-100.

                    Storage Buffer
                    20 mM Tris-HCl (pH8.0), 100mM KCl, 3 mM MgCl2 1mM DTT,0.1% NP-40 ,0.1% Tween20, 0.2mg/ml BSA, 50% (v/v) glycerol

                    Definition of Activity Unit
                    One unit is defined as the amount of the enzyme required to catalyze the incorporation of 10 nM of dNTPs into an acid-insoluble form in 30 minutes at 70°C using hering sperm DNA as substrate.

                    Store all components at -20°C


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