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变性条件下免疫沉淀蛋白的高分辨率等电聚焦。一种应用于补体成分多态性研究的简单分析方法。

High resolution isoelectric focusing of immunoprecipitated proteins under denaturing conditions. A simple analytical method applied to the study of complement component polymorphisms.

作者信息

Rodriguez de Córdoba S, Rubinstein P, Ferreira A

出版信息

J Immunol Methods. 1984 Apr 27;69(2):165-72. doi: 10.1016/0022-1759(84)90314-4.

Abstract

A simple analytical method for the study of structural protein polymorphisms is described. It consists of the immunoprecipitation of non-radiolabeled proteins using monospecific polyclonal antibodies followed by isoelectric focusing (IEF) under completely denaturing conditions in vertical polyacrylamide slab gels. The method uses small amounts of sample (usually unfractionated plasma or serum), requires no sophisticated equipment and allows the screening of large numbers of samples with comparatively small effort. This method has been applied in the identification of 2 human complement-component polymorphisms, C4-binding protein (C4-bp) and factor H (beta 1H).

摘要

本文描述了一种用于研究结构蛋白多态性的简单分析方法。该方法包括使用单特异性多克隆抗体对非放射性标记蛋白进行免疫沉淀,然后在垂直聚丙烯酰胺平板凝胶中完全变性条件下进行等电聚焦(IEF)。该方法使用少量样品(通常为未分级的血浆或血清),无需复杂设备,并且能够以相对较小的工作量筛选大量样品。此方法已应用于鉴定两种人类补体成分多态性,即C4结合蛋白(C4-bp)和因子H(β1H)。

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