Firer M A, Hosking C S, Hill D J
J Immunol Methods. 1981;46(1):31-40. doi: 10.1016/0022-1759(81)90329-x.
This paper describes the development of a simple, sensitive and specific enzyme-linked immunosorbent assay (ELISA) for the measurement of serum IgG, IgA and IgM antibodies to cow's milk protein. The specificity of this assay was determined by preparing immunosorbents of cow's milk and human serum albumin (HSA). Fractionation of the antiserum-enzyme label by gel filtration and affinity chromatography showed that the conjugate preparation contained moieties of antiserum-enzyme, and antiserum-enzyme polymers. The preparation also contained enzyme-enzyme and antiserum-antiserum conjugates. Purification of the labeled reagent did not improve the sensitivity. The reagents and conditions used have been analyzed for purposes of standardisation.
本文描述了一种用于检测血清中抗牛奶蛋白IgG、IgA和IgM抗体的简单、灵敏且特异的酶联免疫吸附测定(ELISA)方法的开发。通过制备牛奶和人血清白蛋白(HSA)免疫吸附剂来确定该测定方法的特异性。通过凝胶过滤和亲和色谱对抗血清 - 酶标记物进行分级分离,结果表明缀合物制剂包含抗血清 - 酶部分以及抗血清 - 酶聚合物。该制剂还包含酶 - 酶和抗血清 - 抗血清缀合物。标记试剂的纯化并未提高灵敏度。已对所使用的试剂和条件进行分析以实现标准化。