نتایج جستجو برای: taq polymerase

تعداد نتایج: 128420  

Journal: :The Journal of biological chemistry 2004
Derek L Ho W Malcolm Byrnes Wu-Po Ma Yuan Shi David J E Callaway Zimei Bu

The DNA polymerase I from Thermus aquaticus (Taq polymerase) performs lagging-strand DNA synthesis and DNA repair. Taq polymerase contains a polymerase domain for synthesizing a new DNA strand and a 5'-nuclease domain for cleaving RNA primers or damaged DNA strands. The extended crystal structure of Taq polymerase poses a puzzle on how this enzyme coordinates its polymerase and the nuclease act...

Journal: :The Biochemical journal 2003
Irene Karantzeni Carmen Ruiz Chin-Chi Liu Vince J Licata

Thermal denaturations of the type 1 DNA polymerases from Thermus aquaticus (Taq polymerase) and Escherichia coli (Pol 1) have been examined using differential scanning calorimetry and CD spectroscopy. The full-length proteins are single-polypeptide chains comprising a polymerase domain, a proofreading domain (inactive in Taq) and a 5' nuclease domain. Removal of the 5' nuclease domains produces...

Journal: :BioTechniques 2000
H Igarashi K Nagura H Sugimura

2.Cusi, M.G., M. Valassina and P.E. Valensin. 1994. Comparison of M-MLV reverse transcriptase and Tth polymerase activity in RTPCR of samples with low virus burden. BioTechniques 17:1034-1036. 3.Fiorenza, M.T. and F. Mangia. 1998. Quantitative RT-PCR amplification of RNA in single mouse oocytes and preimplantation embryos. BioTechniques 24:618-623. 4.Huang, Z., M.J. Fasco and L.S. Kaminsky. 199...

Journal: :Croatian medical journal 2005
Davorka Sutlović Marija Definis Gojanović Simun Andelinović Dijana Gugić Dragan Primorac

AIM To investigate the dose-response effect of humic acid (HA) on the quantitative real time polymerase chain reaction (QRT-PCR) inhibition and the efficiency of Taq polymerase increment in preventing inhibition by HA in DNA extracted from ancient bones. METHODS DNA was isolated from bone samples and DNA quantification was conducted with the real-time 5' exonuclease detection assay (TaqMan), ...

2017
Marcin Olszewski Marta Śpibida Maciej Bilek Beata Krawczyk

DNA polymerases are present in all organisms and are important enzymes that synthesise DNA molecules. They are used in various fields of science, predominantly as essential components for in vitro DNA syntheses, known as PCR. Modern diagnostics, molecular biology and genetic engineering need DNA polymerases which demonstrate improved performance. This study was aimed at obtaining a new NeqSSB-T...

Journal: :BioTechniques 1996
L T Parker H Zakeri Q Deng S Spurgeon P Y Kwok D A Nickerson

Taq DNA polymerases in which the phenylalanine is substituted by a tyrosine at position 667 (Taq F667Y) are members of a new class of DNA polymerases that incorporate chain-terminating dideoxyribonucleoside triphosphates (ddNTPs) much more efficiently than the wild-type Taq DNA polymerase. Improved incorporation of ddNTPs into DNA during cycle sequencing using AmpliTaq DNA polymerase, FS (Taq-F...

Journal: :Nucleic acids research 1992
M M Huang N Arnheim M F Goodman

Thermus aquaticus (Taq) DNA polymerase was used to measure the extension efficiency for all configurations of matched and mismatched base pairs at template-primer 3'-termini. The transition mispairs, A(primer).C, C.A, G.T, and T.G were extended 10(-3) to 10(-4)-fold less efficiently than their correctly paired counterparts. Relative efficiencies for extending transversion mispairs were 10(-4) t...

Journal: :Journal of dairy science 2001
C H Kim M Khan D E Morin W L Hurley D N Tripathy M Kehrli A O Oluoch I Kakoma

Staphylococcus aureus is an economically important and a major mastitis-causing pathogen that also poses food safety and antimicrobial resistance threats. Substances in mastitic milk inhibit the Taq DNA polymerase reaction (Taq PCR) making it of limited use for detecting S. aureus mastitis. In the study reported here, a set of oligonucleotide primers of 21 and 24 bases was used in Taq-PCR to am...

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