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用于自动定量人类DNA的实时定量PCR检测方法的发育验证

Developmental validation of a real-time quantitative PCR assay for automated quantification of human DNA.

作者信息

Richard Melanie L, Frappier Roger H, Newman Jonathan C

机构信息

Biology Section, Centre of Forensic Sciences, Toronto, Ontario, Canada.

出版信息

J Forensic Sci. 2003 Sep;48(5):1041-6.

Abstract

Our laboratory has developed an automated real-time quantitative PCR assay for detecting human DNA. The assay utilizes an in-house, custom-designed TaqMan-MGB sequence-specific probe (CFS-HumRT) and the ABD 7900HT SDS platform. Developmental validation has followed TWGDAM (1) guidelines and demonstrates that the assay is primate specific, is highly sensitive, yields consistent results, and works with human DNA extracted from a variety of body fluid stains. When operating within the dynamic range of the system using high-quality DNA samples. the technique yields similar quantification results to our current QuantiBlot assay with the added benefit of time saving through automation. Furthermore, the QPCR assay identifies how much amplifiable DNA is in a sample and thus has the potential to predict PCR success in downstream applications such as STR analysis.

摘要

我们实验室已开发出一种用于检测人类DNA的自动化实时定量PCR检测方法。该检测方法使用了一种内部定制设计的TaqMan-MGB序列特异性探针(CFS-HumRT)和ABD 7900HT SDS平台。方法学验证遵循了TWGDAM(1)指南,结果表明该检测方法具有灵长类特异性、高度灵敏、结果一致,并且适用于从各种体液污渍中提取的人类DNA。在使用高质量DNA样本并在系统的动态范围内操作时,该技术产生的定量结果与我们当前的QuantiBlot检测方法相似,且通过自动化操作还具有节省时间的额外优势。此外,定量PCR检测方法能够确定样本中可扩增DNA的量,因此有潜力预测下游应用(如STR分析)中的PCR成功率。

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