Fluorometric Polymerase Chain Reaction (PCR) Enzyme-Linked Immunosorbent Assay for Quantification of Immuno-PCR Products in Microplates

1997 ◽  
Vol 246 (1) ◽  
pp. 140-145 ◽  
Author(s):  
Christof M. Niemeyer ◽  
Michael Adler ◽  
Dietmar Blohm
Keyword(s):  
Polymerase Chain Reaction ◽  
Immunosorbent Assay ◽  
Enzyme Linked Immunosorbent Assay ◽  
Chain Reaction ◽  
Pcr Products ◽  
Polymerase Chain

scholarly journals Genotyping ofSalmonellaspp. on the basis of CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)

2018 ◽  
Author(s):  
Calvin Jiksing ◽  
Normah Yusop ◽  
Farhan Nazaie Nasib ◽  
Kenneth Francis Rodrigues
Keyword(s):  
Polymerase Chain Reaction ◽  
Mycobacterium Tuberculosis ◽  
Immunosorbent Assay ◽  
Deoxyribonucleic Acid ◽  
Enzyme Linked Immunosorbent Assay ◽  
Chain Reaction ◽  
Pcr Polymerase Chain Reaction ◽  
Crispr Array ◽  
Polymerase Chain ◽  
Veterinary Laboratory

ABSTRACTAimsBacterial genotyping on the basis of the CRISPR array has been established inMycobacterium tuberculosiswith a method called spacer oligonucleotide typing (spoligotyping). The spoligotyping method had been widely used for both detection and typing ofM. tuberculosiscomplex bacteria. This present study aimed at determining if the CRISPR array inSalmonellaspp. could be applied to establish a correlationship between serogroup and the fingerprint generated by CRISPR typing.Methodology and resultsA total of 30 samples were obtained from Diagnostic Veterinary Laboratory, Kota Kinabalu, Sabah. Serogroup was determined on the basis of ELISA (enzyme-linked immunosorbent assay). Four different serogroups were identified which were serogroup B, C, D, and E. DNA (deoxyribonucleic acid) was extracted and PCR (polymerase chain reaction) was performed using primers which were designed to amplify the CRISPR array inSalmonellagenome. Our results indicate that there is a correlationship between serogroup obtained using ELISA and the profile generated by CRISPR typing.Conclusion, significance and impact of studyCRISPR typing has the potential to be applied for the genotyping ofSalmonella.

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