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.
