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一种利用¹²⁵I标记蛋白A的结合进行病毒抗体放射免疫测定的方法。

A radioimmunoassay for virus antibody using binding of 125I-labelled protein A.

作者信息

Colombatti A, Hilgers J

出版信息

J Gen Virol. 1979 May;43(2):395-401. doi: 10.1099/0022-1317-43-2-395.

Abstract

An assay for virus antibodies using protein A from Staphylococcus aureus is described. Type B and type C RNA tumour viruses adsorbed on to polystryrene microtitre plate wells were incubated with antiserum and then with 125I-labelled protein A (I-pA) and bound radioactivity was determined. Technical details such as labelling, antigen concentration, storage of I-pA are reported. The specificity of the reaction was investigated in detail by competition experiments with purified unbound homologous viruses. This assay also proved to be sensitive for demonstration of autogenous immunity to both type B and type C RNA tumour viruses. A study using antisera against purified core and envelope virus proteins of mammary tumour and leukaemis viruses suggested that the reaction mainly involves surface antigens of the intact virions.

摘要

本文描述了一种使用金黄色葡萄球菌蛋白A检测病毒抗体的方法。吸附在聚苯乙烯微量滴定板孔上的B型和C型RNA肿瘤病毒先与抗血清孵育,然后与125I标记的蛋白A(I-pA)孵育,测定结合的放射性。报告了标记、抗原浓度、I-pA储存等技术细节。通过与纯化的未结合同源病毒进行竞争实验,详细研究了反应的特异性。该检测方法还被证明对检测针对B型和C型RNA肿瘤病毒的自身免疫敏感。一项使用针对乳腺肿瘤病毒和白血病病毒纯化核心蛋白和包膜蛋白的抗血清的研究表明,该反应主要涉及完整病毒粒子的表面抗原。

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