Use of a monoclonal antibody to estrone-3-glucuronide in an enzyme-linked immunosorbent assay (ELISA)

Peter A. Elder, Laurette Manley, John G. Lewis
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引用次数: 11

Abstract

A direct urinary ELISA for estrone-3-glucuronide has been produced following cloning and characterisation of a monoclonal antibody to the above estrogen metabolite. The ELISA follows our established pattern of absorbing a thyroglobulin conjugate, to which estrone-3-glucuronide has been coupled, to the wells of a microtitre plate using guanidine hydrochloride. A competition reaction between either standards/samples and the adsorbed hormone compete for antibody combining sites. The assay is completed by addition of an antimouse Ig-peroxidase complex and read at 492 nm following additions of O -phenylenediamine substrate in under 4 h. The correlation between urinary “total estradiol” and “total estrone and estradiol” is very good and, in conjunction with our ELISA for pregnanediol glucuronide, has allowed for the improved clinical management of infertile and subfertile women.

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雌激素-3-葡萄糖醛酸单克隆抗体在酶联免疫吸附试验(ELISA)中的应用
在克隆和鉴定了上述雌激素代谢物的单克隆抗体后,产生了针对雌激素-3-葡萄糖醛酸盐的直接尿ELISA。ELISA遵循我们建立的模式,吸收甲状腺球蛋白偶联物,雌二醇-3-葡萄糖醛酸盐偶联,到微滴板的孔使用盐酸胍。标准品/样品和吸附的激素之间的竞争反应会竞争抗体结合位点。该检测通过添加抗小鼠igg过氧化物酶复合物完成,并在添加O -苯二胺底物后在492 nm处读取,用时不到4小时。尿液“总雌二醇”和“总雌酮和雌二醇”之间的相关性非常好,并且与我们的妊娠二醇葡萄糖醛酸苷酶联免疫吸附试验相结合,可以改善不孕和不孕妇女的临床管理。
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