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Application of PCR-ELISA in Molecular Diagnosis

Polymerase chain reaction-enzyme linked immunosorbent assay (PCR-ELISA) is an immunodetection method that can quantify PCR product directly after immobilization of biotinylated DNA on a microplate. This method, which detects nucleic acid instead of protein, is a much more sensitive method compared t...

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Detalles Bibliográficos
Autores principales: Sue, Mei Jean, Yeap, Swee Keong, Omar, Abdul Rahman, Tan, Sheau Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058250/
https://www.ncbi.nlm.nih.gov/pubmed/24971343
http://dx.doi.org/10.1155/2014/653014
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author Sue, Mei Jean
Yeap, Swee Keong
Omar, Abdul Rahman
Tan, Sheau Wei
author_facet Sue, Mei Jean
Yeap, Swee Keong
Omar, Abdul Rahman
Tan, Sheau Wei
author_sort Sue, Mei Jean
collection PubMed
description Polymerase chain reaction-enzyme linked immunosorbent assay (PCR-ELISA) is an immunodetection method that can quantify PCR product directly after immobilization of biotinylated DNA on a microplate. This method, which detects nucleic acid instead of protein, is a much more sensitive method compared to conventional PCR method, with shorter analytical time and lower detection limit. Its high specificity and sensitivity, together with its semiquantitative ability, give it a huge potential to serve as a powerful detection tool in various industries such as medical, veterinary, and agricultural industries. With the recent advances in PCR-ELISA, it is envisaged that the assay is more widely recognized for its fast and sensitive detection limit which could improve overall diagnostic time and quality.
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spelling pubmed-40582502014-06-26 Application of PCR-ELISA in Molecular Diagnosis Sue, Mei Jean Yeap, Swee Keong Omar, Abdul Rahman Tan, Sheau Wei Biomed Res Int Review Article Polymerase chain reaction-enzyme linked immunosorbent assay (PCR-ELISA) is an immunodetection method that can quantify PCR product directly after immobilization of biotinylated DNA on a microplate. This method, which detects nucleic acid instead of protein, is a much more sensitive method compared to conventional PCR method, with shorter analytical time and lower detection limit. Its high specificity and sensitivity, together with its semiquantitative ability, give it a huge potential to serve as a powerful detection tool in various industries such as medical, veterinary, and agricultural industries. With the recent advances in PCR-ELISA, it is envisaged that the assay is more widely recognized for its fast and sensitive detection limit which could improve overall diagnostic time and quality. Hindawi Publishing Corporation 2014 2014-05-27 /pmc/articles/PMC4058250/ /pubmed/24971343 http://dx.doi.org/10.1155/2014/653014 Text en Copyright © 2014 Mei Jean Sue et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Sue, Mei Jean
Yeap, Swee Keong
Omar, Abdul Rahman
Tan, Sheau Wei
Application of PCR-ELISA in Molecular Diagnosis
title Application of PCR-ELISA in Molecular Diagnosis
title_full Application of PCR-ELISA in Molecular Diagnosis
title_fullStr Application of PCR-ELISA in Molecular Diagnosis
title_full_unstemmed Application of PCR-ELISA in Molecular Diagnosis
title_short Application of PCR-ELISA in Molecular Diagnosis
title_sort application of pcr-elisa in molecular diagnosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058250/
https://www.ncbi.nlm.nih.gov/pubmed/24971343
http://dx.doi.org/10.1155/2014/653014
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