Taq DNA Polymerase is routinely used for PCR applications in molecular biology. Taq products from Edna have exceptional activity, stability and value in terms of cost per unit. Learn more in the Product Data Sheet and Brochure with product information, detailed usage protocols and sample gel results.
Available in TDP-80 (400 U), TDP-200 (1000 U), TDP-400 (2000 U) formats
Taq DNA Polymerase is a thermostable DNA polymerase that has 5´→ 3´ polymerase activity and 5´ flap endonuclease activity. Edna Taq products are recombinantly produced in E. coli and thus are highly pure and offer robust and reliable PCR activity.
What's In The Box:
The product includes a vial of the formulated recombinant enzyme along with 10X Taq reaction buffer which is detergent-free and designed to be compatible with existing assay systems.
Highlights:
Isolated from a recombinant source
The enzyme is free of any tags
Supplied with 10X Reaction Buffer
Robust and reliable reactions
Tolerates a wide range of templates
Incorporates dUTP, dITP and fluorescently-labeled nucleotides
An ideal tool for amplifying DNA of length <5 kb
Product Source
An E. coli strain that carries the Taq DNA Polymerase gene from Thermus aquaticus.
Unit Definition: One unit is defined as the amount of enzyme that will incorporate 15 nmol of dNTP into acid-insoluble material in 30 minutes at 75°C.
Storage Temperature: -20 C
Molecular Weight: 94 kDa
Activity: 5'-3' exonuclease (not 3'-5') resulting in single-base 3' overhangs
Heat Inactivation: None
10x Taq Reaction Buffer:
100 mM Tris-HCl
500 mM KCl
15 mM MgCl2
(pH 8.3)
Edna Taq DNA Polymerase products are well suited to a range of molecular biology applications:
Polymerase Chain Reaction (PCR)
Primer Extension
Colony PCR
Microarray Analysis
DHPLC
High-fidelity Pfu DNA Polymerase with 10x Buffer (Mg-free) and MgCl2
T4 DNA Ligase Standard Concentration with 10x Ligation Buffer
EdnaBeads Plasmid DNA Extraction Kit (Coming Soon!)
EdnaBeads DNA Clean-Up Kit (Coming Soon!)
Extra Buffers and Reagents for Molecular Biology (for Taq DNA Polymerase, Pfu DNA Polymerase, RNase A, and T4 DNA Ligase reactions)