Our proprietary DB SuperSens Taq and DB AptaTaq DNA Polymerases deliver robust and precise amplification across a wide range of PCR workflows. Designed for both routine and high-demanding applications, they combine high thermostability, sensitivity and specificity. Available as colorless and green ready-to-load formulations.
Interested in our portfolio? We created the complete catalogue of our PCR and RT-PCR mixes, enzymes and inhibitors. Find everything you need in one place. Download it HERE.
PRODUCTS
DB AptaTaq DNA Polymerase
Gold standard for your PCR and RT-PCR applications. Perfect for routine PCR amplification, high throughput PCR, TA cloning, and DNA labeling
DB AptaTaq DNA Polymerase Green
Gold standard for your PCR and RT-PCR applications and ready to load. Perfect for routine PCR amplification, high throughput PCR, TA cloning, and DNA labeling
DB SuperSens Taq DNA Polymerase
Ensure excellent results in your PCR and RT-PCR applications with DB SuperSens Taq DNA Polymerase. Perfect for routine PCR amplification, high throughput PCR, TA cloning, and DNA labeling
DB SuperSens Taq DNA Polymerase Green
Ensure excellent results in your PCR and RT-PCR applications with DB SuperSens Taq DNA Polymerase. Perfect for routine PCR amplification, high throughput PCR, TA cloning, and DNA labeling with ready to load option.
DNA Polymerase [Discontinued]
Ensure excellent results in your PCR and RT-PCR applications with DB AptaTaq DNA Polymerase. Perfect for routine PCR amplification, high throughput PCR, TA cloning, and DNA labeling
Key Parameters
Our enzymes provide superior stability, efficiency, and simplicity ensuring reliable results for every experiment.
Possess intrinsic 5’-3’ polymerase, 5’-3’ exonuclease and 5’ flap activities for various molecular biology applications.
Supplied with a complete reaction buffer with enhancers, stabilizers, and optimal concentration of metal ions and dNTPs.
Recombinant enzymes with a half-life of over 40 min at 95 °C suitable for amplification of DNA up to 5 kb.
Suitable for real-time PCR from cDNA, genomic DNA, plasmid DNA or synthesis of DNA templates for T/A cloning.
Eva Mlynarčíková
Lead Developer in PCR chemistry
