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Validation of a Real-Time PCR On-Site Quantification Method for MON810 Maize

  • Stephen R.H. Langrell
  • , Theodore R. Allnutt
  • , Valérie Laval
  • , Yves Bertheau
  • , Maria Pla
  • , Nina Papazova
  • , David Lee
  • European Commission Joint Research Centre Institute
  • Fera Science Ltd.
  • INRAE
  • Research Institute for Agriculture and Fisheries
  • National Institute of Agricultural Botany

Research output: Contribution to journalScientific articlepeer-review

Abstract

A 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%).

Original languageEnglish
Pages (from-to)313-318
Number of pages6
JournalFood Analytical Methods
Volume4
Issue number3
DOIs
Publication statusPublished - Sept 2011

Keywords

  • Adventitious genetically modified (GM) presence (AGMP)
  • Co-existence monitoring
  • Detection
  • Duplex RT-PCR
  • MON810
  • On-site
  • Portable

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