… has been mixed in, according to U.S. Patent 5,436,149. KlentaqLA (KTLA) or TaqLA or TthLA are the best enzymes for … plain water at room temperature. * 10xKLA for Klentaq1, KlentaqLA, and Taquenase is * 500 mM Tris-HCl pH 9.2; 160 mM … For PCR targets under 2 kb, 1/2 as much enzyme (TaqLA or KlentaqLA) is needed if the extension temperature is lowered …
… N-terminal deletion (removing the 5'-[flap]exonuclease of Taq DNA polymerase). PCR tests show that Klentaq1 has … thermostability (about 2 degrees) relative to wild-type Taq, and it gives higher yields of amplicon. We speculate … were performed in duplicate. A competitor Hot Start Taq was also included. The PCR reactions were stored at 4°C …
… Each tube of 1.5 ml of 10x Klentaq1 Reaction Buffer pH 9.2 is enough for 600 25 ul PCR reactions. 10x buffer … 0.5% Brij 58, and 35 mM magnesium chloride. Our 10x Klentaq1 Reaction Buffer pH 7.9 also available for better … Datasheet Klentaq1 Reaction Buffer 9.2 …
… Hot Start Cesium Klentaq C LA is made with aptamer-based technology, enabling room … dUTP. 10x buffer composition is: 500 mM Tris-Cl pH 9.2, 160 mM ammonium sulfate, 0.25% Brij 58, and 35 mM … Datasheet HS Cesium Klentaq C LA … Klentaq … SDS- HS Cesium Klentaq C LA …
… 10x Klentaq1 Reaction Buffer pH 7.9 is enough for 600 25ul PCR reactions. 10x buffer composition is 500 mM Tris-Cl, 160 … specifically for Klentaq1. It is distinct from the Klentaq Mutant Reaction Buffer that is designed for CesiumKlentaq, Omni Klentaq, and other Klentaq mutants. …
… A lyoph-ready preparation of Cesium Klentaq AC, a double cold-sensitive mutant of Klentaq1 … is designed for hot start PCR performance. Since Cesium Klentaq AC lacks 5' exonuclease activity, it is not suitable … assays.10x buffer composition is: 500 mM Tris-Cl pH 9.2, 160 mM ammonium sulfate, 0.25% Brij 58, and 35 mM …
… of the following enzymes: Klentaq1 OmniTaq OmniTaq 2 OmniTaq 3 Omni Klentaq Omni Klentaq 2 Cesium Klentaq AC Cesium Klentaq C CesiumTaq ZipTaq … Reverse Transcription and PCR in One … Faster PCR …
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