Application of PCR-ELISA in Molecular Diagnosis

Joint Authors

Tan, Sheau Wei
Sue, Mei Jean
Omar, Abdul Rahman
Yeap, Swee Keong

Source

BioMed Research International

Issue

Vol. 2014, Issue 2014 (31 Dec. 2014), pp.1-6, 6 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2014-05-27

Country of Publication

Egypt

No. of Pages

6

Main Subjects

Medicine

Abstract EN

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.

American Psychological Association (APA)

Sue, Mei Jean& Yeap, Swee Keong& Omar, Abdul Rahman& Tan, Sheau Wei. 2014. Application of PCR-ELISA in Molecular Diagnosis. BioMed Research International،Vol. 2014, no. 2014, pp.1-6.
https://search.emarefa.net/detail/BIM-488497

Modern Language Association (MLA)

Sue, Mei Jean…[et al.]. Application of PCR-ELISA in Molecular Diagnosis. BioMed Research International No. 2014 (2014), pp.1-6.
https://search.emarefa.net/detail/BIM-488497

American Medical Association (AMA)

Sue, Mei Jean& Yeap, Swee Keong& Omar, Abdul Rahman& Tan, Sheau Wei. Application of PCR-ELISA in Molecular Diagnosis. BioMed Research International. 2014. Vol. 2014, no. 2014, pp.1-6.
https://search.emarefa.net/detail/BIM-488497

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-488497