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用于呼吸道合胞病毒的单克隆捕获抗体酶联免疫吸附测定:检测单个病毒抗原及确定单克隆抗体特异性

Monoclonal capture antibody ELISA for respiratory syncytial virus: detection of individual viral antigens and determination of monoclonal antibody specificities.

作者信息

Hendry R M, Fernie B F, Anderson L J, Godfrey E, McIntosh K

出版信息

J Immunol Methods. 1985 Mar 18;77(2):247-58. doi: 10.1016/0022-1759(85)90037-7.

Abstract

An enzyme-linked immunosorbent assay (ELISA) for respiratory syncytial virus (RSV) that employs solid-phase monoclonal antibodies was developed. RSV antigens bound by these monoclonal capture antibodies were detected by addition of a polyclonal bovine antiserum, followed anti-bovine enzyme conjugate and enzyme substrate. The sensitivity and specific of the assay were determined by titrations of the solid-phase antibodies and by antigen titrations with both unpurified RSV-infected cell culture material and purified RSV nucleocapsids. The addition of a competitive binding step prior to the addition of antigen to the solid-phase antibody provides further evidence of the assay's specificity. Furthermore, the competitive binding assay enables the antigen specificity of monoclonal antibodies to be determined or compared without the use of purified antigens. Monoclonal capture ELISA is a convenient, rapid, and sensitive assay that can be used to measure specific RSV antigens in unpurified preparations as well as to determine anti-RSV antibody specificity and should prove useful in examining other complex antigen-antibody systems.

摘要

开发了一种采用固相单克隆抗体的呼吸道合胞病毒(RSV)酶联免疫吸附测定(ELISA)。通过添加多克隆牛抗血清,随后添加抗牛酶偶联物和酶底物,来检测这些单克隆捕获抗体所结合的RSV抗原。通过滴定固相抗体以及用未纯化的RSV感染细胞培养物和纯化的RSV核衣壳进行抗原滴定,来确定该测定法的灵敏度和特异性。在将抗原添加到固相抗体之前添加竞争结合步骤,进一步证明了该测定法的特异性。此外,竞争结合测定法能够在不使用纯化抗原的情况下确定或比较单克隆抗体的抗原特异性。单克隆捕获ELISA是一种方便、快速且灵敏的测定法,可用于测量未纯化制剂中的特异性RSV抗原,以及确定抗RSV抗体的特异性,并且在检测其他复杂的抗原-抗体系统中应会证明有用。

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