Bioneer HotStart DNA Polymerase with dNTPs (1,000 Units)
SKU: E-3151
Bioneer HotStart DNA Polymerase with dNTPs (1,000 Units)
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HotStart DNA polymerase inhibits PCR by using pyrophosphate (PPi) to trap Mg2+ ions essential for PCR, then breaking the PPi down by using heat resistant enzyme pyrophosphatase (PPase) as the temperature increases while processing the PCR reaction
※This product is shipped in dry ice.
Principles of HotStart DNA Polymerase
HotStart DNA Polymerase is a new concept of DNA polymerase that utilizes chemical interactions between pyrophosphate (PPi) and pyrophosphatase (PPase).
While divalent cation magnesium (Mg2+) plays an important role in PCR, the pyrophosphate binds with Mg2+ to form a complex that inhibits the PCR.
However, the Mg-PPi complex will decompose into Mg2+ and 2Pi by the thermostable pyrophosphatase (PPase) during the PCR reaction, allowing increased reactivity with the by-product of the digested PPi, 2Pi.
Features and Benefits
Sensitivity & Specificity
Reduced generation of non-specific responses and primer-dimer formation during the mixing of PCR components by inhibiting DNA polymerase activity at the room temperature
Efficiency
Improved yield of target DNA through its high sensitivity and specificity
Reproducibility
Reproducible results with uniform quality products for each batch under the ISO 9001 quality system
Applications
- HotStart PCR, PCR with complex genomic templates/low copy templates/cDNA
- Multiplex PCR
- Primer extension
- SNP typing
- Real-time PCR using dsDNA Binding dye
- Multiple primer pairs and amplification of low copy template DNA
Specifications
5' to 3' exonuclease activity | No |
3' to 5' exonuclease activity | No |
3' – A overhang | Yes |
Fragment size | Up to 12 kb |
Components
10X reaction buffer : Tris-HCl, KCl, Pyrophosphate, pH 9.0
1X dilution buffer : 50% glycerol containing 50 mM Tris-HCl, 0.1 mM EDTA, 1 mM DTT, stabilizers, pH 8.2
10 mM dNTPs mix : 2.5 mM of each dNTP
20 mM MgCl2
Concentration
250 Units (5U/μl)
Storage Conditions
50% glycerol containing 20 mM Tris-HCl, 0.5 mM EDTA, 1 mM DTT, 100 mM KCl, stabilizers, pH 8.0.
Storage Temperature
-20°C
Unit Definition
One unit is defined at the amount of enzyme that will incorporate 10 nmole of dNTP into acid-insoluble material in 30 minutes at 72°C.