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通过酶联免疫吸附测定(ELISA)进行Gm分型。

Gm typing by enzyme-linked immunosorbent assay (ELISA).

作者信息

Kishda T, Tamaki Y

出版信息

Z Rechtsmed. 1984;93(1):23-7. doi: 10.1007/BF00202980.

Abstract

A solid-phase ELISA for Gm typing is described. A mixture of anti-Gm serum (or monoclonal anti-Gm antibody) and test serum was incubated in microtiter wells coated with IgG or its fragments of appropriate Gm type. After washing of the wells, the bound antibody was detected with peroxidase-labeled second antibody. The Glm(3), G3m(16), and G3m(21) antigens could be identified by this technique. Since some of the human anti-Gm sera and anti-Rh0 sera required for the conventional hemagglutination-inhibition method are hard to obtain, the ELISA system using anti-Gm antibodies and no anti-Rh0 sera may serve as an alternative to the conventional method.

摘要

本文描述了一种用于Gm分型的固相酶联免疫吸附测定法(ELISA)。将抗Gm血清(或单克隆抗Gm抗体)与检测血清的混合物在包被有适当Gm型IgG或其片段的微量滴定孔中孵育。孔洗涤后,用辣根过氧化物酶标记的二抗检测结合的抗体。用该技术可鉴定Glm(3)、G3m(16)和G3m(21)抗原。由于传统血凝抑制法所需的一些人抗Gm血清和抗Rh0血清难以获得,使用抗Gm抗体且无需抗Rh0血清的ELISA系统可作为传统方法的替代方法。

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