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Development of dual priming oligonucleotide-polymerase chain reaction (DPO-PCR) for detection of wheat component in foods

机译:促进双灌注寡核苷酸聚合酶链反应(DPO-PCR),用于检测食物中的小麦组分

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摘要

This research is aimed to establish a DPO-PCR method for rapid detection of wheat component in foods. A pair of highly specific DPO primers was designed using the wheat housekeeping gene GAG56D as the target gene. By optimizing the PCR reaction system, the DPO-PCR detection method for wheat component in food was established, and the specificity and sensitivity of the method were determined. The established DPO-PCR method was highly specific, and there was no cross-reactivity to 22 control samples. The sensitivity was high, and the minimum detection limit was 1 ng/uL. Tests on commercially available product samples showed that the method can effectively detect wheat component of foods. The DPO-PCR method established in this study is simple and accurate, and provides an effective detection method for wheat component in foods.
机译:该研究旨在建立一种用于快速检测食物中小麦组分的DPO-PCR方法。 使用小麦管家基因Gag56D作为靶基因设计了一对高度特异性DPO引物。 通过优化PCR反应体系,确定了小麦组分的DPO-PCR检测方法,确定了该方法的特异性和灵敏度。 所建立的DPO-PCR方法具有高度特异性,并且没有与22种对照样品的交叉反应性。 灵敏度高,最小检测限为1 ng / ul。 在市售产品样品上的测试表明该方法可以有效地检测食物的小麦成分。 本研究中建立的DPO-PCR方法简单且准确,并为食物中的小麦组分提供了有效的检测方法。

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