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Validation of a real-time PCR on-site quantification method for MON810 maize
Version 2 2024-06-17, 19:33Version 2 2024-06-17, 19:33
Version 1 2016-10-10, 10:14Version 1 2016-10-10, 10:14
journal contribution
posted on 2024-06-17, 19:33 authored by SRH Langrell, TR Allnutt, V Laval, Y Bertheau, M Pla, N Papazova, D LeeA rapid on-, or near-site, quantitative method for use as a pre-harvest predictive decision, or co-existence monitoring, tool for adventitious genetically modified (GM) presence has been developed. Based on a laboratory-based protocol for real-time (RT) quantification of the MON810 GM event in maize kernels, the duplex RT polymerase chain reaction method was constructed around the portable Cepheid SmartCyclerII platform, requiring only modest support infrastructure for field application. Validation through an international ring trial showed good compliance with minimum assay performance requirements as defined by the European Network of GMO Laboratories (RSD r=18.5%; RSD R=32.8; Bias=26.7%). © 2010 Springer Science+Business Media, LLC.
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Journal
Food analytical methodsVolume
4Pagination
313-318Location
Berlin, GermanyPublisher DOI
ISSN
1936-9751eISSN
1936-976XLanguage
engPublication classification
C Journal article, C1.1 Refereed article in a scholarly journalCopyright notice
2010, Springer Science+Business Media, LLCIssue
3Publisher
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