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通过酶联免疫吸附测定法对gp41抗原进行比较分析,以检测抗1型人类免疫缺陷病毒抗体。

Comparative analysis of gp41 antigens by enzyme-linked immunosorbent assays for detecting antibodies to human immunodeficiency virus type 1.

作者信息

Zweig M, Bladen S V, Dubois G C, Samuel K P, Showalter S D, Papas T S

机构信息

Program Resources, Inc., National Cancer Institute-Frederick Cancer Research Facility, MD.

出版信息

AIDS Res Hum Retroviruses. 1988 Dec;4(6):487-92. doi: 10.1089/aid.1988.4.487.

Abstract

We have compared the antigenic qualities of human immunodeficiency virus type 1 (HIV-1) gp41 glycoprotein with a synthetic oligopeptide (peptide R21S) and a bacterially synthesized protein (protein 566), which are homologous with the N-terminal region of gp41, in enzyme-linked immunosorbent assays (ELISA) for detecting antibodies to HIV-1 in sera of patients with the acquired immunodeficiency syndrome (AIDS) or the aids-related complex (ARC). Although the use of all three types of antigens readily allowed the detection of antibodies in human sera, ELISA employing purified gp41 glycoprotein and the protein 566 were more specific and sensitive than the peptide R21S ELISA.

摘要

我们在酶联免疫吸附测定(ELISA)中,比较了1型人类免疫缺陷病毒(HIV-1)糖蛋白gp41与一种合成寡肽(肽R21S)和一种细菌合成蛋白(蛋白566)的抗原特性,这两种物质与gp41的N端区域同源,用于检测获得性免疫缺陷综合征(AIDS)或艾滋病相关综合征(ARC)患者血清中的HIV-1抗体。尽管使用这三种抗原都能很容易地检测出人类血清中的抗体,但采用纯化的gp41糖蛋白和蛋白566的ELISA比肽R21S ELISA更具特异性和敏感性。

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