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STR DNA分型:通过减少PCR反应体积提高灵敏度并有效消耗样本

STR DNA typing: increased sensitivity and efficient sample consumption using reduced PCR reaction volumes.

作者信息

Leclair Benoît, Sgueglia Joanne B, Wojtowicz Patricia C, Juston Ann C, Frégeau Chantal J, Fourney Ron M

机构信息

National DNA Data Bank, Royal Canadian Mounted Police, 1200 Vanier Parkway, Ottawa, Ontario, Canada.

出版信息

J Forensic Sci. 2003 Sep;48(5):1001-13.

Abstract

Improvements in detection limits/sensitivity and lower sample consumption are potential benefits of reducing PCR reaction volumes used in forensic DNA typing of crime scene samples. This premise was studied first with experimental mixtures and a nine-loci megaplex, which demonstrated stochiometric amplification and accurate detection. Next, adjudicated casework samples were subjected to amplification under 15 different template DNA to PCR reaction volume ratios. Reduction of PCR reaction volume and DNA down to 10 microL and 0.500 ng, respectively, produced identical profiles with the same signal intensity and heterozygous allele peak height ratio (HR). Reduction to 5 microL and 0.063 ng yielded HR values that were slightly affected in one to three STR loci. PCR reaction volume reduction can enhance detection and sensitivity while reducing the consumption of irreplaceable crime scene samples.

摘要

在犯罪现场样本的法医DNA分型中,降低PCR反应体积可能带来检测限/灵敏度的提高以及样本消耗的减少。首先用实验混合物和一个九位点复合扩增体系对这一假设进行了研究,结果表明存在化学计量扩增和准确检测。接下来,对已裁决的案件样本在15种不同的模板DNA与PCR反应体积比下进行扩增。将PCR反应体积和DNA分别降至10微升和0.500纳克时,产生了具有相同信号强度和杂合等位基因峰高比(HR)的相同图谱。降至5微升和0.063纳克时,在一到三个STR位点的HR值受到轻微影响。减少PCR反应体积可以提高检测和灵敏度,同时减少不可替代的犯罪现场样本的消耗。

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