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               <dc:title>Multiplex Polymerase Chain Reaction-Capillary Gel Electrophoresis: A Promising Tool for GMO ScreeningAssay for Simultaneous Detection of Five Genetically Modified Cotton Events and Species</dc:title>
               <dc:creator>Nadal i Matamala, Anna</dc:creator>
               <dc:creator>Esteve Nuez, Teresa</dc:creator>
               <dc:creator>Pla i de Solà-Morales, Maria</dc:creator>
               <dc:subject>Reacció en cadena de la polimerasa</dc:subject>
               <dc:subject>Plantes transgèniques</dc:subject>
               <dc:subject>Cotó</dc:subject>
               <dc:subject>Polymerase chain reaction</dc:subject>
               <dc:subject>Transgenic plants</dc:subject>
               <dc:subject>Cotton</dc:subject>
               <dc:description>A multiplex polymerase chain reaction assay coupled to capillary gel electrophoresis for amplicon identification by size and color (multiplex PCR-CGE-SC) was developed for simultaneous detection of cotton species and 5 events of genetically modified (GM) cotton. Validated real-time-PCR reactions targeting Bollgard, Bollgard II, Roundup Ready, 3006-210-23, and 281-24-236 junction sequences, and the cotton reference gene acp1 were adapted to detect more than half of the European Union-approved individual or stacked GM cotton events in one reaction. The assay was fully specific (&lt;1.7% of false classification rate), with limit of detection values of 0.1% for each event, which were also achieved with simulated mixtures at different relative percentages of targets. The assay was further combined with a second multiplex PCR-CGE-SC assay to allow simultaneous detection of 6 cotton and 5 maize targets (two endogenous genes and 9 GM events) in two multiplex PCRs and a single CGE, making the approach more economic. Besides allowing simultaneous detection of many targets with adequate specificity and sensitivity, the multiplex PCR-CGE-SC approach has high throughput and automation capabilities, while keeping a very simple protocol, e.g., amplification and labeling in one step. Thus, it is an easy and inexpensive tool for initial screening, to be complemented with quantitative assays if necessary</dc:description>
               <dc:date>2025-01-15T23:06:20Z</dc:date>
               <dc:date>2025-01-15T23:06:20Z</dc:date>
               <dc:date>2009-05-01</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:type>peer-reviewed</dc:type>
               <dc:identifier>http://hdl.handle.net/10256/25939</dc:identifier>
               <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1093/jaoac/92.3.765</dc:relation>
               <dc:relation>info:eu-repo/semantics/altIdentifier/issn/1060-3271</dc:relation>
               <dc:relation>info:eu-repo/semantics/altIdentifier/eissn/1944-7922</dc:relation>
               <dc:rights>Tots els drets reservats</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Oxford University Press</dc:publisher>
               <dc:source>© Journal of AOAC International, 2009, vol. 92, núm. 3, p. 765-772</dc:source>
               <dc:source>Articles publicats (D-EQATA)</dc:source>
               <dc:source>Nadal i Matamala, Anna Esteve Nuez, Teresa Pla i de Solà-Morales, Maria 2009 Multiplex Polymerase Chain Reaction-Capillary Gel Electrophoresis: A Promising Tool for GMO ScreeningAssay for Simultaneous Detection of Five Genetically Modified Cotton Events and Species Journal of AOAC International 92 3 765 772</dc:source>
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