TaqNovaHS DNA Polymerase is a mixture of thermostable Taq DNA polymerase and a highly specific monoclonal antibody, which acts as an inhibitor of the polymerization activity (for Hot-Start PCR technique); high PCR specificity with minimal optimization; fast 3-minute enzyme activation time; very efficient
|RP925A||2500 U ( 5U/μl )||Ask for an offer|
|RP910A||1000 U ( 5 U/μl )||Ask for an offer|
|RP905A||500 U ( 5U/μl )||Ask for an offer|
|RP902A||200 U ( 5U/μl )||Ask for an offer|
TaqNovaHS Polymerase is a mixture of thermostable Taq DNA polymerase isolated from Thermus aquaticus and a highly specific monoclonal antibody, which acts as an inhibitor of the polymerization activity. The TaqNovaHS enables easy set-up of a hot-start PCR reaction at room temperature. The antibody binds reversibly to the enzyme, inhibiting polymerase activity at ambient temperatures, which prevents extension of non-specifically annealed primers and primer-dimers formed at low temperatures during PCR setup. The antibody is released from the polymerase during normal cycling conditions. The use of the TaqNovaHS Polymerase does not require any additional incubation step to activate the enzyme.
It is recommended for a wide range of demanding applications, which require highly specific amplification. The TaqNovaHS polymerase is a universal and easy-to-use DNA polymerase which works rapidly and effectively in various PCR conditions. The enzyme catalyses DNA synthesis in a 5’ → 3’ direction, shows no 3′ → 5’ exonuclease activity, but has a 5’ → 3’ exonuclease activity.
Features and advantages
- High PCR specificity with minimal optimization
- Minimizes amplification of non-specific products and primer-dimers
- Fast 3-minute enzyme activation time
- Suitable for a wide range of applications
- Increased yield of PCR products
- Amplifies fragments of up to 5 kb
- Leaves ´A´ overhangs
- Hot-start PCR
- Singleplex and multiplex PCR
- Real-Time PCR
- Diagnostic PCR with DNA from various kinds of specimen
- Specific amplification of difficult templates (GC-rich)
One unit is defined as an amount of enzyme required to incorporate 10 nmol of dNTPs to an insoluble DNA fraction in 30 minutes at 75°C in a 50 μl reaction.
TaqNovaHS DNA Polymerase (RP9) - Manual
20 mM Tris-HCl (pH 8.0, 25°C), 100 mM KCl, 0.1 mM EDTA, 1 mM DTT, 0.5% (v/v) Nonidet P40, 0.5% (v/v) Tween 20, 50% (v/v) glycerol.
Store all components at -20°C.
Shipping on dry or blue ice.
Free of nonspecific nucleases (DNases) contamination. Extensively tested in PCR reactions.
TaqNovaHS DNA Polymerase (RP9) - MSDS
TaqNovaHS DNA Polymerase (RP9) - L. 706472
TaqNovaHS DNA Polymerase (RP9) - L. TGZ626074
TaqNovaHS DNA Polymerase (RP9) - L. TGZ835775
TaqNovaHS DNA Polymerase (RP9) - L. 665673
Genetic diversity and differentiation of alpine salamanders from the Dinarides – an evolutionary perspective with insights for species conservation
Authors Emina Šunje, Ana Zuazu Bermejo, Raoul Van Damme, Thierry Backeljau, Naris Pojskić, Lada Lukić Bilela, Belma Kalamujić Stroil Products TaqNovaHS DNA Polymerase (RP9) Year 2021 Source Salamandra 57(1): 75–88
Development and Cytomolecular Identification of Monosomic Alien Addition and Substitution Lines of Triticale (× Triticosecale Wittmack) With 2S k Chromosome Conferring Leaf Rust Resistance Derived From Aegilops kotschyi Boiss
Authors Michał T. Kwiatek, Waldemar Ulaszewski, Jolanta Belter, Dylan Phillips, Roksana Skowrońska, Aleksandra Noweiska, Halina Wiśniewska Products TaqNovaHS DNA Polymerase (RP9) Year 2020 Source Front Plant Sci. 2020;11:509481
Recovery of 2R.2Sk Triticale-Aegilops kotschyi Robertsonian Chromosome Translocations
Authors Ulaszewski, Waldemar; Belter, Jolanta; Wiśniewska, Halina; Szymczak, Joanna; Skowrońska, Roksana; Phillips, Dylan; Kwiatek, Michał Products TaqNovaHS DNA Polymerase (RP9) Year 2019 Source Agronomy, 9(10), 646