- Reaction speed 5 times faster than standard Taq DNA polymerase
|TaKaRa Z-Taq ||200 U (2.5 U/µL)*|
|10X Z-Taq Buffer (with 30 mM MgCl2)||800 µL|
|dNTP Mixture (2.5 mM each dNTP)||800 µL|
|*1.25 U per 50 µL reaction is recommended|
–20°C. Avoid repeated freezing and thawing of TaKaRa Z-Taq enzyme and dNTPs. Once thawed, aliquot each component and store at –20°C.
PCR products generated with TaKaRa Z-Taq contain a mixture of 3'-A overhangs and blunt ends, allowing >80% cloning efficiency when using T-vectors.
Performance is assessed by rapid PCR amplification of a 10 kb lambda DNA target.