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Analytical Methods for The Detection of Genetically Modified Organisms (GMO) in Food - Prerequisites and Factors Ensuring High Quality Standards

机译:食品中转基因生物(GMO)检测的分析方法-确保高质量标准的前提和因素

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摘要

Since the first attempts to establish analytical methods for the detection of GMO in the food chain mainly DNA (PCR)- and protein based techniques have been developed for this purpose. Whereas protein based techniques - either in a plate format (ELISA to be used in an analytical lab) or so called dip sticks (to be used on site and with almost no equipment necessary) determine the presence of the engineered protein in a sample derived analyte, DNA-based techniques detect the modified or newly integrated DNA sequences. The presentation will focus mainly on DNA detection methods, which are based on PCR techniques. PCR can either be used as simple qualitative screening and identification tools. or, when an additional endogenous reference gene detection system is included in the PCR assay, may also be used for quantification of the relative GMO content under conditions of varying matrix properties. Reliable GMO detection however needs more than only the appropriate core analytical procedure consisting of sample preparation, (DNA-) extraction and subsequent PCR analysis. Major factors influencing analytical quality and meaningful interpretation of results obtained at different stages will be highlighted in the following chapters.
机译:自首次尝试建立用于检测食物链中转基因生物的分析方法以来,为此目的主要开发了基于DNA(PCR)和蛋白质的技术。而基于蛋白质的技术-以平板形式(用于分析实验室的ELISA)或所谓的浸涂棒(可在现场使用,几乎不需要任何设备)确定样品衍生的分析物中是否存在工程蛋白质。 ,基于DNA的技术可检测修饰的或新整合的DNA序列。演讲将主要集中在基于PCR技术的DNA检测方法上。 PCR可以用作简单的定性筛选和鉴定工具。或者,当PCR分析中包含其他内源参照基因检测系统时,也可以在基质特性变化的条件下对相对GMO含量进行定量。但是,可靠的GMO检测不仅需要适当的核心分析程序,还包括样品制备,(DNA-)提取和后续PCR分析。在接下来的章节中将重点介绍影响分析质量和有意义地解释在不同阶段获得的结果的主要因素。

著录项

  • 来源
    《》|2002年|p.110-112|共3页
  • 会议地点 Beijing(CN);Beijing(CN)
  • 作者

    Andreas Wurz;

  • 作者单位

    GeneScan Analytics GmbH, Engesserstr. 4b, 79108 Freiburg Germany;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 农作物;
  • 关键词

  • 入库时间 2022-08-26 14:28:40

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