Detail:
Series: Methods in Molecular Biology | Volume: 1542 | Pub. Date: Dec-11-2016 | Page Range: 293-309 | DOI: 10.1007/978-1-4939-6707-0_19
Year prepared: 2016
Multiplex PCR-based methods for simultaneous detection and quantification of different mycotoxin-producing Penicillia are useful tools to be used in food safety programs. These rapid and sensitive techniques allow taking corrective actions during food processing or storage for avoiding accumulation of mycotoxins in them. In this chapter, three multiplex PCR-based methods to detect at least patulin- and ochratoxin A-producing Penicillia are detailed. Two of them are different multiplex real-time PCR suitable for monitoring and quantifying toxigenic Penicillium using the nonspecific dye SYBR Green and specific hydrolysis probes (TaqMan). All of them successfully use the same target genes involved in the biosynthesis of such mycotoxins for designing primers and/or probes.
url: Access via Springer ProtocolsLaboratory Protocols
-
Title
Type
-
Fungal Molecular Biology
-
Susceptibility testing
-
Additional methods & reference
-
Detection in clinical samples
-
Detection in clinical samples
-
Biochemical Calculators
-
Aztec Labs Diagnostic testing Protocols
-
Aztec Labs Diagnostic testing Protocols
-
Aztec Labs Diagnostic testing Protocols
-
Aztec Labs Diagnostic testing Protocols