Literature DB >> 1368485

Simultaneous amplification and detection of specific DNA sequences.

R Higuchi1, G Dollinger, P S Walsh, R Griffith.   

Abstract

We have enhanced the polymerase chain reaction (PCR) such that specific DNA sequences can be detected without opening the reaction tube. This enhancement requires the addition of ethidium bromide (EtBr) to a PCR. Since the fluorescence of EtBr increases in the presence of double-stranded (ds) DNA an increase in fluorescence in such a PCR indicates a positive amplification, which can be easily monitored externally. In fact, amplification can be continuously monitored in order to follow its progress. The ability to simultaneously amplify specific DNA sequences and detect the product of the amplification both simplifies and improves PCR and may facilitate its automation and more widespread use in the clinic or in other situations requiring high sample throughput.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1368485     DOI: 10.1038/nbt0492-413

Source DB:  PubMed          Journal:  Biotechnology (N Y)        ISSN: 0733-222X


  165 in total

1.  Quantification of ammonia-oxidizing bacteria in arable soil by real-time PCR.

Authors:  A Hermansson; P E Lindgren
Journal:  Appl Environ Microbiol       Date:  2001-02       Impact factor: 4.792

2.  Detection and quantification of protein phosphatase inhibitor-1 gene expression in total rat liver and isolated hepatocytes.

Authors:  E A Aleem; T Flohr; A Hunziker; D Mayer; P Bannasch; H W Thielmann
Journal:  Mol Cell Biochem       Date:  2001-01       Impact factor: 3.396

3.  Transcript quantitation in total yeast cellular RNA using kinetic PCR.

Authors:  J J Kang; R M Watson; M E Fisher; R Higuchi; D H Gelfand; M J Holland
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

4.  Branch migration inhibition in PCR-amplified DNA: homogeneous mutation detection.

Authors:  A Lishanski; N Kurn; E F Ullman
Journal:  Nucleic Acids Res       Date:  2000-05-01       Impact factor: 16.971

5.  A new label technology for the detection of specific polymerase chain reaction products in a closed tube.

Authors:  J Nurmi; A Ylikoski; T Soukka; M Karp; T Lövgren
Journal:  Nucleic Acids Res       Date:  2000-04-15       Impact factor: 16.971

6.  A fluorescent quantitative PCR approach to map gene deletions in the Drosophila genome.

Authors:  P W Chiang; W L Wei; K Gibson; R Bodmer; D M Kurnit
Journal:  Genetics       Date:  1999-11       Impact factor: 4.562

7.  Making sense of polymer-based biosensors.

Authors:  P S Heeger; A J Heeger
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-26       Impact factor: 11.205

Review 8.  High-throughput SNP genotyping with the Masscode system.

Authors:  M Kokoris; K Dix; K Moynihan; J Mathis; B Erwin; P Grass; B Hines; A Duesterhoeft
Journal:  Mol Diagn       Date:  2000-12

9.  PCR bias in ecological analysis: a case study for quantitative Taq nuclease assays in analyses of microbial communities.

Authors:  S Becker; P Böger; R Oehlmann; A Ernst
Journal:  Appl Environ Microbiol       Date:  2000-11       Impact factor: 4.792

10.  Detection of Herpes simplex virus DNA by real-time PCR.

Authors:  H H Kessler; G Mühlbauer; B Rinner; E Stelzl; A Berger; H W Dörr; B Santner; E Marth; H Rabenau
Journal:  J Clin Microbiol       Date:  2000-07       Impact factor: 5.948

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.