Literature DB >> 8074881

TaqStart Antibody: "hot start" PCR facilitated by a neutralizing monoclonal antibody directed against Taq DNA polymerase.

D E Kellogg1, I Rybalkin, S Chen, N Mukhamedova, T Vlasik, P D Siebert, A Chenchik.   

Abstract

The specificity and DNA yield of PCRs are often improved by the "hot start" technique and analogous methods. The intent of the approach is to eliminate or prevent the generation of nonspecific PCR templates that may be synthesized at ambient temperature prior to thermal cycling. Monoclonal antibodies (MAbs) raised in mice to the purified DNA polymerase of Thermus aquaticus (Taq) were selected for their ability to reversibly block polymerase activity. The MAbs, incubated with Taq DNA polymerase and added to PCR tubes at ambient temperature, yield specific DNA fragments upon amplification when using high numbers of temperature cycles and a very low copy number of target DNA in a complex DNA background. This approach, using the TaqStart Antibody, permits the preparation of reaction mixtures at ambient temperatures without the subsequent opening of reaction tubes, use of grease or waxes, or of degradative enzymes and deoxyribonucleotide analogs.

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Year:  1994        PMID: 8074881

Source DB:  PubMed          Journal:  Biotechniques        ISSN: 0736-6205            Impact factor:   1.993


  38 in total

1.  Development of a PCR assay for rapid detection of enterococci.

Authors:  D Ke; F J Picard; F Martineau; C Ménard; P H Roy; M Ouellette; M G Bergeron
Journal:  J Clin Microbiol       Date:  1999-11       Impact factor: 5.948

2.  Digital PCR.

Authors:  B Vogelstein; K W Kinzler
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

3.  PCR hot start using primers with the structure of molecular beacons (hairpin-like structure).

Authors:  O K Kaboev; L A Luchkina; A N Tret'iakov; A R Bahrmand
Journal:  Nucleic Acids Res       Date:  2000-11-01       Impact factor: 16.971

4.  A new class of homogeneous nucleic acid probes based on specific displacement hybridization.

Authors:  Qingge Li; Guoyan Luan; Qiuping Guo; Jixuan Liang
Journal:  Nucleic Acids Res       Date:  2002-01-15       Impact factor: 16.971

5.  Cold-sensitive mutants of Taq DNA polymerase provide a hot start for PCR.

Authors:  Milko B Kermekchiev; Anatoly Tzekov; Wayne M Barnes
Journal:  Nucleic Acids Res       Date:  2003-11-01       Impact factor: 16.971

Review 6.  Specificity and performance of PCR detection assays for microbial pathogens.

Authors:  Konrad Sachse
Journal:  Mol Biotechnol       Date:  2004-01       Impact factor: 2.695

Review 7.  Improved PCR method for amplification of GC-rich DNA sequences.

Authors:  F Hubé; P Reverdiau; S Iochmann; Y Gruel
Journal:  Mol Biotechnol       Date:  2005-09       Impact factor: 2.695

8.  Evaluation of PCR assays in presence of antibody to thermostable DNA polymerases for detection of microbial agents: avoiding false negative results for specimen containing low-titer agent.

Authors:  S K Poddar; M H Sawyer; J D Connor
Journal:  J Clin Lab Anal       Date:  1998       Impact factor: 2.352

9.  The Dlx gene complement of the leopard shark, Triakis semifasciata, resembles that of mammals: implications for genomic and morphological evolution of jawed vertebrates.

Authors:  David W Stock
Journal:  Genetics       Date:  2004-10-16       Impact factor: 4.562

10.  Selective control of primer usage in multiplex one-step reverse transcription PCR.

Authors:  Elena Hidalgo Ashrafi; Joyclyn Yee; Natasha Paul
Journal:  BMC Mol Biol       Date:  2009-12-30       Impact factor: 2.946

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