Our Publications | DNA Polymerase Technology

A Single Amino Acid Change to Taq DNA Polymerase Enables Faster PCR, Reverse Transcription and Strand-Displacement
https://doi.org/10.3389/fbioe.2020.553474
A Conservative Isoleucine to Leucine Mutation Causes Major Rearrangements and Cold Sensitivity in Klentaq1 DNA Polymerase
http://pubs.acs.org/doi/pdf/10.1021/bi501198f
OmniTaq and Omni Klentaq: Mutants of Taq DNA polymerase resistant to PCR inhibitors allow DNA amplification from whole blood and crude soil samples
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2655666/
PCR Enhancer Cocktails (PEC): Direct DNA Amplification from Crude Clinical Samples Using a PCR Enhancer Cocktail and Novel Mutants of Taq. http://www.journals.elsevierhealth.com/periodicals/jmdi/article/S1525-1578%2810%2960043-8/fulltext
CesiumTaq and Cesium Klentaq: Cold-sensitive mutants of Taq DNA polymerase provide a hot start for PCR
Nucleic Acids Research. 2003; 31(21): 6139-6147.
RockStart: Magnesium precipitate hot start method for PCR.
Mol Cell Probes. 2002 Jun;16(3):167-71.Molecular and Cellular Probes, 2002.
Klentaq and KlentaqLA: PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC43341/