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美国国家标准与技术研究院标准参考物质2372人类DNA定量标准品的生产与认证。

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

作者信息

Kline Margaret C, Duewer David L, Travis John C, Smith Melody V, Redman Janette W, Vallone Peter M, Decker Amy E, Butler John M

机构信息

Biochemical Science Division, National Institute of Standards and Technology, 100 Bureau Drive, MS 8311, Gaithersburg, MD 20899-8311, USA.

出版信息

Anal Bioanal Chem. 2009 Jun;394(4):1183-92. doi: 10.1007/s00216-009-2782-0. Epub 2009 Apr 18.

Abstract

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.

摘要

法医人类身份鉴定领域使用的现代高度多重短串联重复序列(STR)检测方法要求在聚合酶链反应(PCR)过程中对扩增的样本DNA初始量进行严格控制。这反过来又需要能够可重复地测量样本提取物中人类DNA的浓度[DNA]。定量PCR(qPCR)技术可以在极小的样本中确定特定核苷酸序列的完整DNA片段数量;然而,这些检测必须用成分明确且稳定的DNA提取物进行校准。到2004年,由美国国家标准与技术研究院(NIST)协调或向其报告的研究表明,一种成分明确、稳定的人类DNA定量认证参考物质(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。为确保能够监测这种定量标准的稳定性,并且在需要时能够制备等效的替代材料,需要测量与[DNA]直接相关的某种稳定量。利用在260nm处光密度(正确地称为十分衰减)与水溶液中[DNA]之间长期确立的传统关系,NIST标准参考物质(SRM)2372人类DNA定量标准于2007年10月发布。该SRM由三种截然不同的DNA提取物组成:单源男性、多源女性以及男性和女性来源的混合物。所有三种SRM成分的光密度非常相似,因此传统[DNA]也非常相似。这些材料在几种广泛使用的中性性别检测中表现非常相似,表明适当的制备方法和计量合理的分光光度测量相结合,能够制备和认证既可持续又具有实际用途的定量[DNA]标准。

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