DNA Polymerases

AccuTaq &#8482 long and accurate (LA) DNA Polymerase is a combination of Taq DNA polymerase with a small amount of a polymerase with the 3′&#85945′ exonuclease activity necessary for proofreading. It enables the amplification of genomic

AccuTaq &#8482 long and accurate (LA) DNA Polymerase is a combination of Taq DNA polymerase with a small amount of a polymerase with the 3′&#85945′ exonuclease activity necessary for proofreading. It enables the amplification of genomic

AccuTaq &#8482 long and accurate (LA) DNA Polymerase is a combination of Taq DNA polymerase with a small amount of a polymerase with the 3′&#85945′ exonuclease activity necessary for proofreading. It enables the amplification of genomic

DNA polymerase beta (EC 2.7.

POLG is a mitochondrial protein that plays a major role in mitochondrial DNA replication and only for mitochondrial DNA. POLG is the catalytic subunit of a multiple protein complex that makes up the holo-enzyme that is the mitochondrial specific

Anti-POLK polymerase (DNA directed) kappa, 100ul UN 1687 6.1

Anti-POLK polymerase (DNA directed) kappa, 25ul UN 1687 6.1

Bsu DNA Polymerase I, Large Fragment is a product of the Bacillus subtilis DNA polymerase I which lacks the N-terminal exonuclease domain (1-296 amino acids). It retains the 5&acute&rarr 3&acute polymerase activity of DNA polymerase I but lacks

Cheetah&trade Taq is a chemically modified hot-start Taq DNA polymerase useful for preventing or reducing nonspecific DNA amplification in PCR. Modified using a novel modifying reagent, Cheetah&trade Taq represents a major improvement upon

DNA polymerase I (holoenzyme) has 5&#8242&#85943&#8242 and 3&#8242&#85945&#8242 exonuclease activities in addition to its synthetic activity. This bifunctional activity enables the enzyme to use nicks or gaps in double stranded DNA as

DNA polymerase I (holoenzyme) has 5&#8242&#85943&#8242 and 3&#8242&#85945&#8242 exonuclease activities in addition to its synthetic activity. This bifunctional activity enables the enzyme to use nicks or gaps in double stranded DNA as

DNA polymerase I yields two fragments (small and large) upon protease digestion. The large fragment (Klenow fragment) loses the 5&#8242 exonuclease activity that is present in the intact holoenzyme.