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Our Publications

  • 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.
    Proc Natl Acad Sci U S A. 1994 March 15; 91(6): 2216–2220.

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