DX/DT Taq DNA polymerase (Glycerol Free) is a highly thermostable DNA polymerase which is ubiquitously used for PCR reactions. The optimal optimization activity for Taq Polymerase is around 72°C. The enzyme catalyzes 5’ 3’ DNA synthesis but does not possess 3’ 5’ exonuclease activity for proof reading. The storage buffer doesn't contain Glycerol.

The enzyme is anactive at ambient temperatures due to binding of anti Taq antibody. Initital PCR step should be 95℃ for 2 minutes to activate the Taq.