Taq DNA polymerase is a thermostable polymerase derived from the gene of Thermus aquaticus YT1 expressed and purified from Escherichia coli .
※This product is shipped in dry ice.
Features and Benefits
Efficiency & Sensitivity
High efficiency and sensitivity to the templates
Optimized buffer delivery
Stable PCR reaction by providing buffers optimized for the enzyme
Reproducibility
Reproducible results with uniform quality products for each batch by manufacturing under the ISO 9001 quality system
Application
Real-time quantification of DNA and cDNA targets using dual probe and dsDNA binding dye
Gene expression profiling
Microbial & viral pathogen detection
Specifications
5' to 3' exonuclease activity
Yes
3' to 5' exonuclease activity
No
3' – A overhang
Yes
Fragment size
Up to 10 kb
Components
• 10X reaction buffer with (or without) MgCl2: Tris-HCl, KCl, 15 mM MgCl2, pH 9.0
• Dilution buffer: 20 mM Tris-HCl, 0.5 mM EDTA, 1 mM DTT, 100 mM KCl, Stablizers, 50% Glycerol, pH 8.0
• 10 mM dNTPs mix: 2.5 mM of each dNTP
▶ Concentration
500 units (5 U/μl)
▶ Storage conditions
20 mM Tris-HCl, 0.5 mM EDTA, 1 mM DTT, 100 mM KCl, Stablizers, 50% Glycerol pH 8.0
▶ Unit Definition
One unit is defined as the amount of enzyme required to incorporate 10 nmol of dNTP into acid-insoluble material in 30 minutes at 72℃.