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首页> 外文期刊>Journal of Clinical Microbiology >Problems in detection of cytomegalovirus in urine samples by dot blot hybridization.
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Problems in detection of cytomegalovirus in urine samples by dot blot hybridization.

机译:通过斑点印迹杂交检测尿液样本中巨细胞病毒的问题。

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摘要

A hybridization assay for the detection of cytomegalovirus (CMV) in urine specimens was established. Two different DNA fragments were used as hybridization probes: the HindIII L fragment (11.7 kilobases) and the EcoRI J fragment (10.6 kilobases) of the human CMV strain AD169. These probes were used in an isolated and highly purified form and therefore did not cross hybridize with vector sequences. As shown by hybridization with DNA from CMV-infected and uninfected cells, the assay was highly CMV specific and sensitive (detection limit, 750 to 500 fg of CMV DNA). A total of 122 urine specimens were examined by DNA hybridization, virus isolation, and the detection of CMV-induced early nuclear protein. The results coincided in 91% of the samples. The application of DNA hybridization to urine samples, however, is not without problems, and some of the pitfalls and drawbacks are discussed.
机译:建立了一种用于检测尿液标本中巨细胞病毒(CMV)的杂交检测方法。两种不同的DNA片段用作杂交探针:人CMV株AD169的HindIII L片段(11.7千碱基)和EcoRI J片段(10.6千碱基)。这些探针以分离的和高度纯化的形式使用,因此不与载体序列交叉杂交。如与来自CMV感染和未感染的细胞的DNA杂交所显示,该测定具有高度CMV特异性和敏感性(检测限为750至500 fg CMV DNA)。通过DNA杂交,病毒分离以及CMV诱导的早期核蛋白的检测,共检查了122个尿液样本。在91%的样品中结果一致。然而,DNA杂交技术在尿液样本中的应用并非没有问题,并且讨论了一些陷阱和缺点。

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