PCRBIO HS Taq DNA Polymerase - 5000 units

Description

PCRBIO HS Taq DNA Polymerase uses the latest developments in polymerase technology and buffer chemistry to enhance PCR speed, yield and specificity.

Whether you need a hot start assay for high-throughput, automated reaction setup or the detection of a low copy number template, PCR Biosystems offers you a robust industry-leading enzyme to meet your needs.

Features:

• Hot start technology for unrivalled detection of low copy number templates
• Increased PCR success rates with amplicons up to 6kb
• Ultra-low background DNA
• Advanced buffer chemistry including Mg and dNTP
• Efficient specific amplification from GC and AT-rich sequences
• High performance under both fast and standard cycling conditions
• Gives increased PCR throughput with existing thermal cyclers
• Stable at 25°C and 37°C for 4 weeks

“Hot start” is a term used to describe the inactivation of a DNA polymerase until the initial activation step at 95°C. Inactivation below 65°C prevents primer dimer formation and non-specific amplification allowing for specific amplification from low copy number target sequences. Our antibody-mediated hot start technology offers improved specificity and sensitivity compared to other methods.

PCRBIO HS Taq DNA Polymerase uses the latest developments in polymerase technology and buffer chemistry to enhance PCR speed, yield and specificity. The enzyme and buffer system are room temperature stable for 4 weeks and give superior PCR performance on complex templates such has mammalian genomic DNA.

PCRBIO HS Taq DNA Polymerase performs consistently well on a broad range of templates (including both GC and AT rich). PCRBIO HS Taq DNA Polymerase production uses an enhanced 12 step purification strategy which includes physical, chemical and enzymatic removal of host DNA.

For added convenience PCRBIO HS Taq DNA Polymerase is also available as a 2x ready mix. PCRBIO HS Taq Mix Red contains a red dye suitable for direct loading and tracking during agarose gel electrophoresis.