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A microarray platform for parallel detection of five transgenic events in foods: A combined polymerase chain reaction - ligation detection reaction - universal array method

机译:用于并行检测食品中五个转基因事件的微阵列平台:聚合酶链反应-连接检测反应-通用阵列方法

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摘要

We recently developed a multiplex polymerase chain reaction (PCR) system for the simultaneous detection of four transgenic maize (MON810, Bt176, Bt11, and GA21), one transgenic soybean (Roundup Ready), and two control genes (lectin and zein). Because PCR can lead to ambiguous interpretations due to low specificity, we have developed the ligation detection reaction (LDR) combined with a universal array as a molecular tool to confirm results of PCR analysis. Here, we describe the PCR-LDR-universal array procedure and demonstrate its specificity in revealing the presence of transgenic DNA in experimental samples, raw materials, and commercial foodstuffs.
机译:我们最近开发了一种多重聚合酶链反应(PCR)系统,用于同时检测四种转基因玉米(MON810,Bt176,Bt11和GA21),一种转基因大豆(Roundup Ready)和两种控制基因(凝集素和玉米醇溶蛋白)。由于低特异性导致PCR可能导致模棱两可的解释,因此我们开发了结合通用阵列作为分子工具的连接检测反应(LDR),以确认PCR分析的结果。在这里,我们描述了PCR-LDR通用阵列程序,并证明了其在揭示实验样品,原材料和商业食品中转基因DNA的存在方面的特异性。

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