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Identification of human brain from a tissue fragment by detection of neurofilament proteins.

机译:通过检测神经丝蛋白从组织片段中识别人脑。

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摘要

We developed a method for identifying human brain from a tissue-like fragment by detection of neurofilament protein (NF) using enzyme-linked immunosorbent assay (ELISA). NF was extracted from 0.1g of organ/tissue homogenized with Tris-HCl buffer (pH 7.2) containing urea, phenylmethylsulfonyl fluoride (PMSF), EDTA and, EGTA. It was necessary to dilute the extract at more than 2(3)-fold to avoid immunosuppression by urea. Positive reaction was always obtained for NF-H in 2(3)-fold diluted extract of brain tissue, however, NF-L and NF-M were not always detected when a brain fragment contained gray matter. Human cerebral white matter could be easily distinguished from other organs/tissues by detecting any of the NF-subunits. Brains of human and some animals could be discriminated by detecting NF-L or NF-M, although the species specificity of NF-H was not good. Our findings suggested that detection of NF-H was more useful than NF-L and NF-M for identifying a brain from a tissue-like fragment. The present ELISA method for NF-H could identify human brain specimens under the following conditions: putrefied at 4 degrees C for up to 3 weeks, dried at 37 degrees C for at least 4 months, heated at 50 degrees C for at least 4 weeks. Our results showed that our method is useful for identification of brain tissue in forensic stain analysis. Two practical cases are described.
机译:我们开发了一种通过使用酶联免疫吸附测定(ELISA)检测神经丝蛋白(NF)从组织样片段中识别人脑的方法。从0.1g的器官/组织中提取NF,该器官/组织用含尿素,苯甲基磺酰氟(PMSF),EDTA和EGTA的Tris-HCl缓冲液(pH 7.2)匀浆。有必要将提取物稀释至2(3)倍以上,以避免被尿素免疫抑制。在脑组织的2(3)倍稀释稀​​释液中,总能获得针对NF-H的阳性反应,但是,当脑碎片中含有灰质时,总不能检测到NF-L和NF-M。通过检测任何NF-亚基,可以容易地将人脑白质与其他器官/组织区分开。尽管NF-H的物种特异性不好,但可以通过检测NF-L或NF-M来区分人和某些动物的大脑。我们的发现表明,从组织样片段中鉴定出大脑时,NF-H的检测比NF-L和NF-M更有用。当前的NF-H ELISA方法可以在以下条件下鉴定人脑标本:在4摄氏度下腐烂长达3周,在37摄氏度下干燥至少4个月,在50摄氏度下加热至少4周。我们的结果表明,我们的方法可用于鉴定法医染色分析中的脑组织。描述了两种实际情况。

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