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首页> 外文期刊>Forensic science international. Genetics >Proximity Ligation Real-Time PCR: A protein-based confirmatory method for the identification of semen and sperm cells from sexual assault evidence
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Proximity Ligation Real-Time PCR: A protein-based confirmatory method for the identification of semen and sperm cells from sexual assault evidence

机译:接近结扎实时PCR:一种基于蛋白质的确认方法,用于鉴定来自性侵犯证据的精液和精子细胞

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摘要

The positive identification of seminal fluids in sexual assault crimes is considered crucial evidence to determine whether a sexual act occurred or not. However, current presumptive methods lack specificity and sensitivity. Confirmation of semen by microscopic examination of spermatozoa is laborious, time consuming, and can sometimes lead to negative or inconclusive results. Here we report the use of the Proximity Ligation Real-Time PCR (PLiRT-PCR) assay as an attractive and promising confirmatory method for the identification of semen and sperm proteins using two polyclonal antibodies, Prostate Specific Antigen (PSA) and Sperm-Specific Protein (SP10), respectively. PLiRT-PCR, relies on protein recognition by pairs of proximity probes (antibody-DNA conjugates) that give rise to a ligated DNA strand. The ligated DNA strand is then amplified and detected by qPCR.
机译:性侵犯犯罪中的精髓液体的阳性鉴定被认为是重要的证据,以确定是否发生了性行为。 然而,目前的推定方法缺乏特异性和敏感性。 通过微观检查精子的微观检查确认精液是费力,耗时的,有时可以导致消极或不确定的结果。 在这里,我们报告使用邻近连接实时PCR(PLITT-PCR)测定作为使用两个多克隆抗体,前列腺特异性抗原(PSA)和特殊蛋白质的精液和精子蛋白质的吸引力和有前途的确认方法 (SP10)分别。 普利特-PCR,依赖于通过引起连接的DNA链的近距离探针(抗体-DNA缀合物)对蛋白质识别。 然后通过QPCR扩增连接的DNA链并检测。

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