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西特斯公司HLA DQα法医脱氧核糖核酸(DNA)扩增及分型试剂盒的盲法试验报告

Report of the blind trial of the Cetus Amplitype HLA DQ alpha forensic deoxyribonucleic acid (DNA) amplification and typing kit.

作者信息

Walsh P S, Fildes N, Louie A S, Higuchi R

机构信息

Cetus Corp., Emeryville, CA.

出版信息

J Forensic Sci. 1991 Sep;36(5):1551-6.

PMID:1955839
Abstract

The AmpliType HLA DQ alpha forensic DNA amplification and typing kit is designed for the qualitative analysis of the human leukocyte antigen (HLA) DQ alpha alleles present in deoxyribonucleic acid (DNA) extracted from forensic samples. The AmpliType kit is the first forensic DNA typing product based on the GeneAmp polymerase chain reaction (PCR) process. The kit was evaluated by five forensic science laboratories (test sites) to assess their ability to perform DNA typing using PCR on sample types typically encountered by forensic laboratories. None of the DNA-containing samples was mistyped. Of the 180 DNA-containing samples analyzed, results were reported for 178 (98.9%). Of the 178 samples with results, all were correctly typed. Two sites did not report a result for one sample each. Four of the five laboratories experienced no significant levels of contamination in the DNA-containing samples. At the one site with the highest number of DNA-containing samples with contamination, the typing results were not compromised. This site was able to correct the contamination problem through simple procedural changes and stricter attention to sterile technique. Blank controls were important to monitor contamination. In conclusion, the trial demonstrated that forensic science laboratories are capable of setting up a PCR-based DNA typing laboratory and successfully using the AmpliType HLA DQ alpha forensic DNA amplification and typing kit to analyze forensic samples.

摘要

AmpliType HLA DQα法医DNA扩增分型试剂盒专为定性分析从法医样本中提取的脱氧核糖核酸(DNA)中存在的人类白细胞抗原(HLA)DQα等位基因而设计。AmpliType试剂盒是首个基于GeneAmp聚合酶链反应(PCR)技术的法医DNA分型产品。五个法医学实验室(测试地点)对该试剂盒进行了评估,以评定它们使用PCR技术对法医实验室常见样本类型进行DNA分型的能力。所有含DNA的样本均未出现分型错误。在分析的180个含DNA样本中,有178个(98.9%)报告了结果。在报告结果的178个样本中,所有样本分型均正确。有两个地点各有一个样本未报告结果。五个实验室中有四个在含DNA样本中未出现显著污染情况。在含DNA样本污染数量最多的那个地点,分型结果未受影响。该地点通过简单的程序变更和更严格地注意无菌技术,成功解决了污染问题。空白对照对于监测污染情况很重要。总之,该试验表明,法医学实验室有能力建立一个基于PCR的DNA分型实验室,并成功使用AmpliType HLA DQα法医DNA扩增分型试剂盒分析法医样本。

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