首页> 外文期刊>Journal of Agricultural and Food Chemistry >Real-time quantitative PCR detection of genetically modified Maximizer maize and Roundup Ready soybean in some representative foods.
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Real-time quantitative PCR detection of genetically modified Maximizer maize and Roundup Ready soybean in some representative foods.

机译:实时定量PCR检测某些代表性食品中的转基因Maximizer玉米和Roundup Ready大豆。

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A fast and quantitative method was developed to detect transgenic "Maximizer" maize "event 176" (Novartis) and "Roundup Ready" soybean (Monsanto) in food by real-time quantitative PCR. The use of the ABI Prism 7700 sequence detection system allowed the determination of the amplified product accumulation through a fluorogenic probe (TaqMan). Fluorescent dyes were chosen in such a way as to coamplify total and transgenic DNA in the same tube. Using real-time quantitative PCR, 2 pg of transgenic or total DNA per gram of starting sample was detected in 3 h after DNA extraction and the relative amounts of "Maximizer" maize and "Roundup Ready" soybean in some representative food products were quantified.
机译:开发了一种快速定量的方法,通过实时定量PCR检测食品中的转基因“ Maximizer”玉米“ event 176”(Novartis)和“ Roundup Ready”大豆(Monsanto)。使用ABI Prism 7700序列检测系统可以通过荧光探针(TaqMan)确定扩增产物的积累。选择荧光染料的方式可以在同一试管中共扩增总DNA和转基因DNA。使用实时定量PCR,在DNA提取后3小时内每克起始样品检测到2 pg转基因或总DNA,并对一些代表性食品中“ Maximizer”玉米和“ Roundup Ready”大豆的相对量进行了定量。

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