Features - Only 25 errors per 304 kb when using GC-rich template DNA (as determined by sequence analysis)
- Higher efficiency than standard Taq polymerase
- Capable of amplifying high-GC human genomic DNA targets up to 5 kb
- Fast reaction time due to the increased priming efficiency
- High specificity due to the antibody-mediated hot-start technology
Applications - High fidelity PCR
- High GC content PCR
- Amplification of cDNA libraries
- cDNA cloning for protein expression
Components R044A | | PrimeSTAR HS DNA Polymerase (2.5 U/µL) | 100 µL | | 2X PrimeSTAR GC Buffer (Mg2+)* | 1.7 mL | | dNTP Mixture (2.5 mM each) | 800 µL |
*Mg2+ concentration is 2 mM (2X)
PurityNicking, endonuclease and exonuclease activities are not detected upon incubation of 0.6 µg of supercoiled or lambda-Hind II digested pBR322 DNA with 10 units of PrimeSTAR HS enzyme for 1 hour at 74°C.
Storage–20°C. Storage Buffer: [50 mM Tris-HCL (pH 8.2 at 4°C), 100 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 0.1% Tween 20, 0.1% Nonidet P-40, 50% Glycerol]
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