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Molecular subtyping of Salmonella Typhimurium with multiplex oligonucleotide ligation-PCR (MOL-PCR)

Wuyts, V.
Marchal, K.
Bertrand, Sophie
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Abstract

A multiplex oligonucleotide ligation-PCR (MOL-PCR) assay is a valuable high-throughput technique for the detection of bacteria and viruses, for characterization of pathogens and for diagnosis of genetic diseases, as it allows to combine different types of molecular markers in a high-throughput multiplex assay. A MOL-PCR assay starts with a multiplex oligonucleotide ligation reaction for detection of the molecular marker, followed by a singleplex PCR for signal amplification and analysis of the MOL-PCR products on a Luminex platform. This last step occurs through a liquid bead suspension array in which the MOL-PCR products are hybridized to MagPlex-TAG beads.In this chapter, we describe the complete procedure for a MOL-PCR assay for subtyping of

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2016-07-01
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Humana Press
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Scientific book or chapter
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a, analysi, analysis, AS, bacteria, bead suspension array, Biology, Control, data, detection, Diagnosis, disease, Diseases, Dna, Genetic, Gödel Prime Product, high-throughput assay, IS, Isolation, IT, Luminex, lysis, Marker, Markers, method, methods, MOL-PCR, Molecular, Molecular biology, molecular markers, molecular subtyping, Multiplex assay, ON, pathogen, PCR, PRODUCTS, protocol, S, Salmonella, Salmonella enterica, Salmonella typhimurium, Subtyping, Technique, Type, Viruses
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