1
Department of Biology, Damghan Azad University, Damghan, Iran
2
Department of Biology, Faculty of Science, Imam Hossein University, Tehran, Iran
3
Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran
Abstract
Due to the spread of infectious diseases, the existence of a rapid and sensitive detection method is necessary today. Polymerase chain reaction-enzyme linked immunosorbent assay (PCR-ELISA) is a simple manner for detection of microorganism. For example, bacteria, viruses, fungi and others based on nucleic acid sequence. A large number of samples can be screened by this technique simultaneously, so it is not time consuming and is a quick manner. The high sensitivity and specificity of PCR-ELISA make it a powerful technique by simple laboratory facilities. As a result it can be an excellent substituted manner for analysis and detectionin different various fields.
Tayebeh,F , Nazarian,S , Mirhosseini,S A and Amani,J . (2017). Novel PCR-ELISA Technique as a Good Substitute in Molecular Assay. Journal of Applied Biotechnology Reports, 4(2), 567-672.
MLA
Tayebeh,F , , Nazarian,S , , Mirhosseini,S A , and Amani,J . "Novel PCR-ELISA Technique as a Good Substitute in Molecular Assay", Journal of Applied Biotechnology Reports, 4, 2, 2017, 567-672.
HARVARD
Tayebeh F, Nazarian S, Mirhosseini S A, Amani J. (2017). 'Novel PCR-ELISA Technique as a Good Substitute in Molecular Assay', Journal of Applied Biotechnology Reports, 4(2), pp. 567-672.
CHICAGO
F Tayebeh, S Nazarian, S A Mirhosseini and J Amani, "Novel PCR-ELISA Technique as a Good Substitute in Molecular Assay," Journal of Applied Biotechnology Reports, 4 2 (2017): 567-672,
VANCOUVER
Tayebeh F, Nazarian S, Mirhosseini S A, Amani J. Novel PCR-ELISA Technique as a Good Substitute in Molecular Assay. J Apple Biotechnol Rep. 2017;4(2):567-672.
