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Comparison of three DNA extraction methods for the detection and quantification of GMO in Ecuadorian manufactured food

机译:三种DNA提取方法在厄瓜多尔人工食品中检测和定量转基因生物的比较

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摘要

ObjectivesIn Ecuador, food products need to be labeled if exceeded 0.9% of transgenic content in whole products. For the detection of genetically modified organisms (GMOs), three DNA extraction methods were tested in 35 food products commercialized in Ecuador. Samples with positive amplification of endogenous genes were screened for the presence of the Cauliflower mosaic virus 35S-promoter (P35S) and the nopaline synthase-terminator (Tnos). TaqMan™ probes were used for determination of transgenic content of the GTS 40-3-2 and MON810 events through quantitative PCR (qPCR).
机译:目的在厄瓜多尔,如果整个产品中转基因含量超过0.9%,则需要对食品进行标识。为了检测转基因生物,在厄瓜多尔商业化的35种食品中测试了三种DNA提取方法。筛选具有内源基因阳性扩增的样品中是否存在花椰菜花叶病毒35S启动子(P35S)和胭脂碱合酶终止子(Tnos)。 TaqMan™探针用于通过定量PCR(qPCR)测定GTS 40-3-2和MON810事件的转基因含量。

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