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利用荧光原位杂交和激光显微切割技术鉴定和分离男性细胞,用于性侵犯调查。

Identification and isolation of male cells using fluorescence in situ hybridisation and laser microdissection, for use in the investigation of sexual assault.

作者信息

Murray Caroline, McAlister Colin, Elliott Keith

机构信息

The Forensic Science Service, Trident Court, 2960 Solihull Parkway, Birmingham Business Park, Solihull B37 7YN, UK.

出版信息

Forensic Sci Int Genet. 2007 Dec;1(3-4):247-52. doi: 10.1016/j.fsigen.2007.05.003. Epub 2007 Aug 13.

Abstract

In cases of sexual assault involving an azoospermic assailant, vaginal swabs taken from the victim may fail to provide an autosomal DNA profile with which to search a suspect database, as the signal from any male cells present would be masked by that from the overwhelming number of female cells collected on the swab. Here, we describe a method of visually identifying diploid male cells in such samples using fluorescence in situ hybridisation, and selectively harvesting them by means of laser microdissection. This combination of techniques was tested on 26 post-coital vaginal swabs taken at a range of times after intercourse; the collected cells were then subjected to a simple lysis procedure and DNA was amplified using the AmpFlSTR SGMPlus multiplex under low copy number conditions. Useful DNA profiles were generated from samples taken up to 24h after intercourse.

摘要

在涉及无精子症攻击者的性侵犯案件中,从受害者身上采集的阴道拭子可能无法提供用于搜索嫌疑人数据库的常染色体DNA图谱,因为拭子上采集到的大量女性细胞发出的信号会掩盖任何存在的男性细胞发出的信号。在此,我们描述了一种使用荧光原位杂交在这类样本中目视识别二倍体男性细胞,并通过激光显微切割选择性采集这些细胞的方法。该技术组合在性交后不同时间采集的26份性交后阴道拭子上进行了测试;然后对采集的细胞进行简单的裂解程序,并在低拷贝数条件下使用AmpFlSTR SGMPlus复合扩增试剂盒扩增DNA。在性交后长达24小时采集的样本中生成了有用的DNA图谱。

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