Literature DB >> 7542460

Quantitation of PCR products with chemiluminescence.

C S Martin1, L Butler, I Bronstein.   

Abstract

Quantitative PCR and reverse transcription PCR (RT-PCR) are widely used in biomedical, industrial and other research applications to determine the number of RNA or DNA molecules of a specific type and/or sequence in a sample of interest. We have developed an assay system to accurately quantitate PCR products that utilizes solid-phase capture and an enzyme-linked chemiluminescent detection method. The entire assay is performed in a single tube or microplate well. Biotinylated PCR products are quantitated by capture onto a streptavidin-coated surface, followed by hybridization of an internal fluorescein-labeled oligonucleotide probe and subsequent detection with an anti-fluorescein-alkaline phosphatase conjugate and CSPD chemiluminescent substrate. Light signal is measured in a luminometer. The assay sensitivity enables accurate quantitation of target DNA because the measurement is performed on product generated during the exponential phase of amplification. The broad dynamic range of the assay, which is greater than three orders of magnitude of PCR product concentration, simplifies the determination of the number of amplification cycles necessary for accurate quantitation of target molecules. The PCR-Light system is an ultrasensitive, non-isotopic and rapid assay for PCR product detection that also has general application to solution hybridization assays and other quantitation methods.

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Year:  1995        PMID: 7542460

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


  6 in total

1.  A flexible bioluminescent-quantitative polymerase chain reaction assay for analysis of competitive PCR amplicons.

Authors:  J K Actor; J R Limor; R L Hunter
Journal:  J Clin Lab Anal       Date:  1999       Impact factor: 2.352

2.  Detection of parvovirus B19 DNA in bone marrow cells by chemiluminescence in situ hybridization.

Authors:  M Musiani; A Roda; M Zerbini; G Gentilomi; P Pasini; G Gallinella; S Venturoli
Journal:  J Clin Microbiol       Date:  1996-05       Impact factor: 5.948

3.  Prenatal diagnosis of parvovirus B19-induced hydrops fetalis by chemiluminescence in situ hybridization.

Authors:  M Musiani; P Pasini; M Zerbini; G Gentilomi; A Roda; G Gallinella; E Manaresi; S Venturoli
Journal:  J Clin Microbiol       Date:  1999-07       Impact factor: 5.948

4.  Detection of single-copy genes in DNA from transgenic plants by nonradioactive Southern blot analysis.

Authors:  M S McCabe; J B Power; A M de Laat; M R Davey
Journal:  Mol Biotechnol       Date:  1997-02       Impact factor: 2.695

5.  Rapid detection of Campylobacter coli, C. jejuni, and Salmonella enterica on poultry carcasses by using PCR-enzyme-linked immunosorbent assay.

Authors:  Yang Hong; Mark E Berrang; Tongrui Liu; Charles L Hofacre; Susan Sanchez; Lihua Wang; John J Maurer
Journal:  Appl Environ Microbiol       Date:  2003-06       Impact factor: 4.792

Review 6.  Electrical and electrochemical monitoring of nucleic Acid amplification.

Authors:  Tatsuro Goda; Miyuki Tabata; Yuji Miyahara
Journal:  Front Bioeng Biotechnol       Date:  2015-03-05
  6 in total

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