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Variation Analysis of Seven LightCycler Based Real-Time PCR Systems to Detect Genetically Modified Products (RRS, Bt176, Bt11, Mon810, T25, Lectin, Invertase)

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Rapid Cycle Real-Time PCR — Methods and Applications

Abstract

Foodstuffs, additives, and processing aids which comprise or are derived from more than 1% of genetically modified organisms (GMOs) have to be labeled according to Swiss [1] and EU law [2–4] as GMO products. As cultivation of GMOs is increasing rapidly and the products composed of GMO plants appear more and more on the world market, there is a need for sensitive, specific, and quick detection methods in order to monitor the labeling of foodstuffs. Several qualitative [5–7] as well as quantitative-competitive [8–10] PCR methods already exist. However, quantitative real-time PCR methods, which no longer require internal standards, competitors, time-consuming PCR reactions, and gel electrophoresis have recently appeared [11]. One such system is LightCycler real-time PCR technology. Real-time PCR systems allow the analysis of the samples while amplification is still in progress. Results can be obtained in less than 1 h.

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© 2002 Springer-Verlag Berlin Heidelberg

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Dahinden, I., Zimmermann, A., Liniger, M., Pauli, U. (2002). Variation Analysis of Seven LightCycler Based Real-Time PCR Systems to Detect Genetically Modified Products (RRS, Bt176, Bt11, Mon810, T25, Lectin, Invertase). In: Reischl, U., Wittwer, C., Cockerill, F. (eds) Rapid Cycle Real-Time PCR — Methods and Applications. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-48351-6_25

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  • DOI: https://doi.org/10.1007/978-3-642-48351-6_25

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-48353-0

  • Online ISBN: 978-3-642-48351-6

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