Taq DNA polymerase reagent kit PCRBIO
for PCRfor genotypingfor nucleic acids

Taq DNA polymerase reagent kit - PCRBIO - PCR Biosystems Ltd. - for PCR / for genotyping / for nucleic acids
Taq DNA polymerase reagent kit - PCRBIO - PCR Biosystems Ltd. - for PCR / for genotyping / for nucleic acids
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Characteristics

Type
Taq DNA polymerase
Applications
for PCR, for genotyping, for nucleic acids

Description

PCRBIO Taq DNA Polymerase is an affordable, versatile and robust enzyme for all your everyday PCR applications including genotyping, screening and library construction. An enhanced 12-step purification strategy together with an optimised buffer system enable PCRBIO Taq DNA Polymerase to amplify with the highest speed, yield and specificity. Features Increased PCR success rates with amplicons up to 6kb Ultra low background DNA Advanced buffer chemistry including Mg and dNTPs High yields under standard and fast PCR conditions Efficient specific amplification from complex templates including GC and AT-rich sequences More Information PCRBIO Taq DNA Polymerase is a robust enzyme for all your everyday PCR applications including genotyping, screening and library construction. PCRBIO Taq DNA Polymerase performs consistently well on a broad range of templates including both GC and AT rich. PCRBIO Taq DNA Polymerase has 5’-3’ exonuclease activities, but no 3’-5’ exonuclease (proofreading) activity. The enzyme has the same error rate as wild-type taq DNA polymerase, approximately 1 error per 2.0 x 105 nucleotides incorporated. PCRBIO Taq DNA Polymerase provides the research community with an affordable routine application polymerase that performs to the highest possible standard, with a versatility that allows you to amplify with the highest speed, yield, specificity and consistency on the market. PCR products generated are A-tailed and may be cloned into TA cloning vectors. The enzyme is room temperature stable for 4 weeks and is produced using an enhanced 12 step purification strategy which includes physical, chemical and enzymatic removal of host DNA.

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