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通过斑点杂交和直接测序对可疑样本进行PCR扩增的HLA DQα和DQβ DNA分型。

PCR amplified HLA DQ alpha and DQ beta DNA typed by dot-blot hybridization and direct sequence for suspect.

作者信息

Lee J C, Chang J G

机构信息

Department of Forensic Science, Central Police College, Taipei, Taiwan, R.O.C.

出版信息

J Formos Med Assoc. 1992 May;91(5):483-6.

PMID:1358324
Abstract

For more effective screening of suspects, we combined two methods to individualize the biologic evidence from a crime scene: polymerase chain reaction (PCR) dot-blot hybridization for DNA typing of HLA Dq alpha; and PCR direct sequencing for DNA typing of HLA DQ beta. PCR-DQ alpha was typed by an AmpliType HLA DQ alpha kit from Cetus. PCR-DQ beta was typed by direct sequence using the dideoxy chain termination method. In 20 DNA samples, complete separation was demonstrated by these two polymorphic DNAs. This will be of considerable use in screening suspects in crime investigation work. The sensitivity of PCR is useful for trace evidence, and the rapid results of dot-blot hybridization and the precise results of direct sequencing have significant advantages.

摘要

为了更有效地筛查嫌疑人,我们结合了两种方法来对犯罪现场的生物证据进行个体化分析:用于HLA Dqα基因分型的聚合酶链反应(PCR)斑点杂交法;以及用于HLA DQβ基因分型的PCR直接测序法。PCR-DQα通过Cetus公司的AmpliType HLA DQα试剂盒进行分型。PCR-DQβ通过双脱氧链终止法进行直接测序分型。在20个DNA样本中,这两种多态性DNA实现了完全分离。这在犯罪调查工作中筛查嫌疑人方面将有很大用途。PCR的灵敏度对微量证据很有用,斑点杂交的快速结果和直接测序的精确结果具有显著优势。

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