- 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.
Please see the product's Certificate of Analysis for information about storage conditions, product components, and technical specifications. Please see the Kit Components List to determine kit components. Certificates of Analysis and Kit Components Lists are located under the Documents tab.