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Production and certification of NIST Standard Reference Material 2372 Human DNA Quantitation Standard

机译:NIST标准参考材料2372人类DNA定量标准的生产和认证

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Modern highly multiplexed short tandem repeat (STR) assays used by the forensic human-identity community require tight control of the initial amount of sample DNA amplified in the polymerase chain reaction (PCR) process. This, in turn, requires the ability to reproducibly measure the concentration of human DNA, [DNA], in a sample extract. Quantitative PCR (qPCR) techniques can determine the number of intact stretches of DNA of specified nucleotide sequence in an extremely small sample; however, these assays must be calibrated with DNA extracts of well-characterized and stable composition. By 2004, studies coordinated by or reported to the National Institute of Standards and Technology (NIST) indicated that a well-characterized, stable human DNA quantitation certified reference material (CRM) could help the forensic community reduce within- and among-laboratory quantitation variability. To ensure that the stability of such a quantitation standard can be monitored and that, if and when required, equivalent replacement materials can be prepared, a measurement of some stable quantity directly related to [DNA] is required. Using a long-established conventional relationship linking optical density (properly designated as decadic attenuance) at 260 nm with [DNA] in aqueous solution, NIST Standard Reference Material (SRM) 2372 Human DNA Quantitation Standard was issued in October 2007. This SRM consists of three quite different DNA extracts: a single-source male, a multiple-source female, and a mixture of male and female sources. All three SRM components have very similar optical densities, and thus very similar conventional [DNA]. The materials perform very similarly in several widely used gender-neutral assays, demonstrating that the combination of appropriate preparation methods and metrologically sound spectrophotometric measurements enables the preparation and certification of quantitation [DNA] standards that are both maintainable and of practical utility.
机译:法医身份认同团体使用的现代高度复用的短串联重复序列(STR)分析要求严格控制在聚合酶链反应(PCR)过程中扩增的样本DNA的初始量。反过来,这要求具有可再现地测量样品提取物中人类DNA [DNA]浓度的能力。定量PCR(qPCR)技术可以确定极小的样品中指定核苷酸序列的完整DNA片段的数量;但是,这些测定必须使用特征明确且稳定的DNA提取物进行校准。到2004年,由美国国家标准技术研究院(NIST)协调或向其报告的研究表明,表征良好,稳定的人类DNA定量认证参考材料(CRM)可以帮助法医界减少实验室内和实验室间的定量变异性。为确保可以监测这种定量标准的稳定性,并且在需要时可以制备等效的替代材料,需要测量一些与[DNA]直接相关的稳定量。利用将260 nm处的光密度(正确称为十足衰减)与水溶液中的[DNA]关联起来的悠久的传统关系,NIST标准参考材料(SRM)2372人类DNA定量标准于2007年10月发布。该SRM包括三种完全不同的DNA提取物:单源雄性,多源雌性以及雄性和雌性来源的混合物。这三个SRM组件的光密度都非常相似,因此传统的[DNA]也非常相似。这些材料在几种广泛使用的性别中立化验中的表现非常相似,表明适当的制备方法和计量合理的分光光度法测量相结合,可以制备和认证定量[DNA]标准品,这些标准品既可维护,又具有实用性。

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