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基于聚合酶链式反应检测生的和高度加工食品中的转基因大豆和玉米。

PCR-based detection of genetically modified soybean and maize in raw and highly processed foodstuffs.

作者信息

Tengel C, Schüssler P, Setzke E, Balles J, Sprenger-Haussels M

机构信息

QIAGEN GmbH, Hilden, Germany.

出版信息

Biotechniques. 2001 Aug;31(2):426-9. doi: 10.2144/01312pf01.

Abstract

The PCR method has proved to be an invaluable tool for the specific and sensitive detection of genetically modified material (e.g., Roundup Ready Soybean and Bt-176 "Maximizer" Maize) in foodstuffs. The first step in the procedure, namely the purification of nucleic acids from the sample, is often the deciding factor in the production of meaningful results. In this study, we present two procedures that enable an efficient isolation of trace amounts of genetic material from both raw and highly processed foodstuffs. We show that for optimal, PCR-ready DNA purification from highly processed foodstuffs and PCR inhibitor-rich substances--such as cocoa-containing products--adapted protocols for the QIAGEN QIAamp DNA Stool Mini Kit can be utilized. For complete DNA isolation from raw foodstuffs, a protocol using the DNeasy Plant Mini Kit is presented.

摘要

聚合酶链反应(PCR)方法已被证明是一种用于特异性和灵敏检测食品中转基因物质(如抗草甘膦大豆和Bt - 176“Maximizer”玉米)的宝贵工具。该检测程序的第一步,即从样品中纯化核酸,往往是获得有意义结果的决定性因素。在本研究中,我们介绍了两种程序,它们能够从生的和高度加工的食品中高效分离痕量遗传物质。我们表明,对于从高度加工食品和富含PCR抑制剂的物质(如含可可产品)中进行最佳的、适用于PCR的DNA纯化,可以使用针对QIAGEN QIAamp DNA粪便微型试剂盒的改良方案。对于从生食品中完全分离DNA,我们介绍了一种使用DNeasy植物微型试剂盒的方案。

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