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首页> 外文期刊>Journal of Virological Methods >A simple method for preparing synthetic controls for conventional and real-time PCR for the identification of endemic and exotic disease agents.
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A simple method for preparing synthetic controls for conventional and real-time PCR for the identification of endemic and exotic disease agents.

机译:一种用于常规和实时PCR的合成对照物制备的简单方法,用于鉴定地方性和外来病原体。

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摘要

Medical and veterinary diagnostic and public health laboratories world-wide are increasingly being called upon to introduce molecular diagnostic tests for both endemic and exotic diseases. This demand has accelerated following increasing terrorism fears. Ironically these same concerns have lead to tightening of both import and export controls preventing many laboratories, particularly those outside of the United States, from gaining access to positive control material. This in turn has prevented many laboratories from introducing much needed molecular diagnostic tests. We describe here a generic approach for preparing synthetic DNA or RNA control material for use in either TaqMan or conventional PCR assays. The production of synthetic controls using this approach does not require cloning or special equipment or facilities beyond that found in any laboratory performing molecular diagnostics. The approach significantly reduces the possibility of contamination or erroneously reporting false-positive reactions due to contamination from positive control material. Synthetic controls produced using this approach have been employed in all molecular diagnostic tests performed in our laboratory and are used irrespective of whether we possess the organism or not.
机译:全世界越来越多地要求在世界范围内的医学和兽医诊断与公共卫生实验室引入针对地方病和外来疾病的分子诊断测试。随着对恐怖主义的恐惧日益加剧,这种需求已经加速。具有讽刺意味的是,这些同样的担忧导致进出口管制越来越严格,使许多实验室,特别是美国以外的实验室无法获得阳性对照材料。反过来,这阻止了许多实验室引入急需的分子诊断测试。我们在这里描述了一种通用方法,用于制备用于TaqMan或常规PCR分析的合成DNA或RNA对照材料。使用这种方法生产合成质控品不需要克隆或任何专门的设备或设施,而这超出了任何进行分子诊断的实验室所能找到的水平。该方法显着降低了由于阳性对照材料的污染而被污染或错误报告假阳性反应的可能性。使用这种方法产生的合成对照已在我们实验室进行的所有分子诊断测试中使用,并且无论我们是否拥有该生物都可以使用。

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