Our Publications | DNA Polymerase Technology

OmniTaq 2: A Single Amino Acid Change to Taq DNA Polymerase Enables Faster PCR, Reverse Transcription and Strand-Displacement. Front. Bioeng. Biotechnol. 2021 8:553474.
Cesium Klentaq C: A Conservative Isoleucine to Leucine Mutation Causes Major Rearrangements and Cold Sensitivity in Klentaq1 DNA Polymerase. Biochemistry. 2015 54(3):881-9.
OmniTaq and Omni Klentaq: Mutants of Taq DNA polymerase resistant to PCR inhibitors allow DNA amplification from whole blood and crude soil samples Nucleic Acids Res. 2009 37(5): e40.
PCR Enhancer Cocktails (PEC): Direct DNA Amplification from Crude Clinical Samples Using a PCR Enhancer Cocktail and Novel Mutants of Taq. The Journal of Molecular Diagnostics. 2010 12(2): 152-61.
CesiumTaq and Cesium Klentaq: Cold-sensitive mutants of Taq DNA polymerase provide a hot start for PCR
Nucleic Acids Research. 2003 31(21): 6139-47.
RockStart: Magnesium precipitate hot start method for PCR.
Mol Cell Probes. 2002 16(3): 167-71.
Klentaq LA: PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates. Proc Natl Acad Sci U S A. 1994 91(6): 2216-20.
Klentaq1: The fidelity of Taq polymerase catalyzing PCR is improved by an N-terminal deletion. Gene. 1992 112(1): 29-35.