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Hot Start Taq DNA Polymerase (Chemical modification)
- High specifity, chemically modified polymerase activity is completely blocked below 80℃, can be activated by heat treatment at 95°C for 10 min
- High sensitivity with the minimum detection of 0.1 pg DNA
- Comes in the Master Mix form for convenient use
- Applicable for PCR using the dUTP/UDG system
- Suitable for multiple PCR systems
Hot Start Taq DNA Polymerase( Chemical modification ) is a hot-start thermostable DNA polymerase from Thermus aquaticus YT-1, which possesses a 5´→ 3´ polymerase activity and a 5´ flap endonuclease activity. The Hot Start Taq DNA polymerase is chemically modified form Taq DNA polymerase, to increase specificity, sensitivity, and yield
Storage and transportation:
Storage at -20℃ and transportation≤0℃
Supplied in: 10 mM Tris-HCl (pH 8.0 at 25℃), 100 mM KCl, 0.1 mM EDTA, 1 mM dithiothreitol, 0.5% Tween20, 0.5% IGEPAL CA-630 and 50% Glycerol.
Unit definition: One unit is defined as the amount of enzyme that will incorporate 15nmol of dNTP into acid insoluble material in 30 minutes at 75°C.
Quality Control Assays
- Endonuclease Activity: Incubation of 20 U of enzyme with 4 μg pUC19 DNA for 4 hours at 37°C resulted in no detectable degradation of the DNA as determined by gel electrophoresis.
- 5 kb Lambda PCR: 25 Cycles of PCR amplification of 5 ng Lambda DNA with 1.25 units of Taq DNA Polymerase in the presence of 200 µM dNTPs and 0.2 µM primers results in the expected 5 kb product.
- Exonuclease Activity: Incubation of a 50 µl reaction containing a minimum of 12.5 U of Taq DNA Polymerase with 10 nM 5´-FAM oligonucleotide for 30 minutes at 37℃ yields no detectable degradation.
- RNase Activity: Incubation of a 10 µl reaction containing 20 U of enzyme with 1 μg of RNA transcripts for 2 hours at 37°C resulted in no detectable degradation of the RNA as determined by gel electrophoresis.
Heat Inactivation: None
Reaction setup:
a:
b: The optimal concentration of Taq DNA Polymerase may range from 5-50 units/ml (0.1-0.5 units/25 µL reaction) in specialized applications.
Thermocycling Conditions for a Routine 3-Step PCR:
a: An initial denaturation of 1min at 95 °C is sufficient for most amplicons. For complex templates, a longer denaturation of 2–3 min at 95°C is recommended. For colony PCR, an initial 5 min denaturation at 95 °C is recommended.
b: The annealing step is typically 15–60 s. The annealing temperature is based on the Tm of the primer pair and is typically 45–68℃.
The Certificate Of Analysis (COA) & Material Safety Data Sheet (MSDS) Is A Signed Document That Includes The Storage Temperature,
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