Cesium Klentaq C LA

… Cesium Klentaq C LA is a DNA polymerase mixture containing Cesium Klentaq … Long-and-Accurate feature allows amplification of longer products with higher fidelity and accuracy.  LA enzymes are … Datasheet Cesium Klentaq C LA … Klentaq … SDS- Cesium Klentaq C LA …

Hot Start Cesium Klentaq C LA

… Hot Start Cesium Klentaq C LA is made with aptamer-based technology, enabling … Long-Accurate feature allows for amplification of longer products with higher fidelity and accuracy.  LA enzymes are … Datasheet HS Cesium Klentaq C LA … Klentaq … SDS- HS Cesium Klentaq C LA …

10x Klentaq1 Reaction Buffer pH 7.9

… 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 Cesium Klentaq, Omni Klentaq, and other Klentaq mutants. …

Lyoph-Ready Cesium Klentaq AC

… A lyoph-ready preparation of Cesium Klentaq AC, a double cold-sensitive mutant of Klentaq1 … low temperatures this enzyme is designed for hot start PCR performance. Since Cesium Klentaq AC lacks 5' exonuclease … Datasheet GF Cesium Klentaq AC … Klentaq … SDS GF Cesium Klentaq AC …

Enzyme Combo

… Combo allows you to test 10 of our enzymes to see which one works best for your application.  Each combo includes 25 … Reverse Transcription and PCR in One …

Lyoph-Ready Cesium Klentaq C

Cesium Klentaq AC LA

… Cesium Klentaq AC LA is a DNA polymerase mixture containing Cesium Klentaq AC, a double cold-sensitive mutant of Klentaq1 … Datasheet Cesium Klentaq AC LA … Klentaq … SDS- Cesium Klentaq AC LA …

Klentaq LA

… Klentaq LA is for Long and Accurate PCR. It is almost the … enzymes that was the invention of Long PCR (Barnes, 1994). Klentaq LA also has inhibition-resistance properties, … PCR reaction. 8-20 kb should be so easy and reliable with Klentaq LA that we will refund a tube of your purchase if it …

RockStart Performance Data

… OmniTaq 3 and CesiumTaq, in Rockstart buffer or standard PCR buffer. A hot start competitor with aptamer technology was used as a positive control.  PCR reactions were incubated either at 25 degree or 4 degree for 1 hour before PCR cycling.  Results : All full length enzymes show hot …

Lyoph-Ready Klentaq1

… Klentaq …