Bradley M P, Ebensperger C, Wiberg U H
Hum Genet. 1987 Aug;76(4):352-6. doi: 10.1007/BF00272444.
A rapid, sensitive, and reproducible enzyme-linked immunosorbent assay (ELISA), for the detection of the serological sex-specific (Sxs) antigen (formerly termed H-Y antigen; see Introduction), is described. This assay uses bovine testes extract as the solid phase antigen, and high-titer anti-Sxs antisera and a urease-conjugated anti rat-IgG as the first and second antibody respectively. The urea containing substrate causes a pH shift in a positive reaction, which in turn is visualized by the use of bromocresol purple as a pH indicator. The method, and some representative applications of it, are described in detail.
本文描述了一种快速、灵敏且可重复的酶联免疫吸附测定(ELISA)方法,用于检测血清学性别特异性(Sxs)抗原(以前称为H-Y抗原;见引言)。该测定法使用牛睾丸提取物作为固相抗原,分别使用高效价抗Sxs抗血清和脲酶偶联的抗大鼠IgG作为第一抗体和第二抗体。含尿素的底物在阳性反应中会引起pH值变化,进而通过使用溴甲酚紫作为pH指示剂来显现。详细描述了该方法及其一些代表性应用。