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Applicability of Three Alternative Instruments for Food Authenticity Analysis:GMO Identification
Author(s) -
Aaron Burrell,
Chester L. Foy,
Malcolm Burns
Publication year - 2011
Publication title -
biotechnology research international
Language(s) - English
Resource type - Journals
eISSN - 2090-3138
pISSN - 2090-3146
DOI - 10.4061/2011/838232
Subject(s) - capillary electrophoresis , protocol (science) , polymerase chain reaction , identification (biology) , microbiology and biotechnology , genetically modified organism , food science , computational biology , medicine , biology , genetics , gene , pathology , alternative medicine , botany
Ensuring foods are correctly labelled for ingredients derived from genetically modified organisms (GMOs) is an issue facing manufacturers, retailers, and enforcement agencies. DNA approaches for the determination of food authenticitys often use the polymerase chain reaction (PCR), and PCR products can be detected using capillary or gel electrophoresis. This study examines the fitness for purpose of the application of three laboratory electrophoresis instruments (Agilent Bioanalyzer 2100, Lab901 TapeStation, and Shimadzu MCE-202 MultiNA) for the detection of GMOs using PCR based on a previously validated protocol. Whilst minor differences in the performance characteristics of bias and precision were observed, all three instruments demonstrated their applicability in using this protocol for screening of GMO ingredients

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