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用于检测人类免疫缺陷病毒核酸的单克隆抗体溶液杂交试验。

Monoclonal antibody solution hybridization assay for detection of human immunodeficiency virus nucleic acids.

作者信息

Viscidi R P, O'Meara C, Farzadegan H, Yolken R

机构信息

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

J Clin Microbiol. 1989 Jan;27(1):120-5. doi: 10.1128/jcm.27.1.120-125.1989.

Abstract

In this report we describe a novel, nonisotopic hybridization assay for the measurement of viral RNA in biological samples. The assay involved a solution-phase reaction between a biotinylated DNA probe and RNA target sequences. Labeled hybrids were detected in an immunoreaction by using a solid-phase anti-biotin antibody and an enzyme-labeled monoclonal antibody specific for DNA-RNA hybrids. This monoclonal antibody solution hybridization assay was compared with an antigen-capture immunoassay for the detection of human immunodeficiency virus in 436 cell culture samples from 60 seropositive patients. The sensitivity and specificity of the hybridization assay were 93.5 and 94.6%, respectively. Detection of human immunodeficiency virus solely by hybridization in the initial sample but not subsequent samples from seven cultures may reflect detection of virus that was present in the patients' lymphocytes but did not replicate in vitro. Since the assay method is adapatable to the detection of either RNA or DNA, it could provide a means for the detection of a wide range of viral nucleic acids.

摘要

在本报告中,我们描述了一种用于测量生物样品中病毒RNA的新型非同位素杂交检测方法。该检测方法涉及生物素化DNA探针与RNA靶序列之间的溶液相反应。通过使用固相抗生物素抗体和对DNA-RNA杂交体具有特异性的酶标记单克隆抗体,在免疫反应中检测标记的杂交体。将这种单克隆抗体溶液杂交检测方法与抗原捕获免疫检测方法进行比较,以检测来自60名血清阳性患者的436份细胞培养样品中的人类免疫缺陷病毒。杂交检测方法的灵敏度和特异性分别为93.5%和94.6%。仅通过杂交在最初样品中检测到人类免疫缺陷病毒,但在来自七种培养物的后续样品中未检测到,这可能反映了对存在于患者淋巴细胞中但未在体外复制的病毒的检测。由于该检测方法适用于RNA或DNA的检测,它可为检测多种病毒核酸提供一种手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c51/267246/dca646e5b7ca/jcm00061-0147-a.jpg

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