Development of a Microtiter Plate Enzyme-linked Immunosorbent Assay for 17 α, 20 β-21-trihydroxy-4-pregnen-3-one, a Teleost Gondadal Steroid

Development of a Microtiter Plate Enzyme-linked Immunosorbent Assay for 17 α, 20 β-21-trihydroxy-4-pregnen-3-one, a Teleost Gondadal Steroid
复制标题

开发用于 17 α, 20 β-21-三羟基-4-pregnen-3-one(一种硬骨鱼性腺类固醇)的微量滴定板酶联免疫吸附测定法

DOI:
--
复制
发表时间:
1995
期刊:
影响因子:
--
通讯作者:
T. Higashi
T. Higashi
中科院分区:
--
文献类型:
--
作者:
K. Asahina;A. Kambegawa;T. Higashi

文献摘要

被引文献

相似文献

以20ƒÀ-S-3-CMO-horseradish过氧化物酶为标记物和兔培养的同源抗血清,建立了一种简单的固相微滴板酶联免疫吸附测定法(ELISA),用于鉴定诱导硬骨鱼成熟的甾体激素- 17 -¿,20ƒÀ, 21-三羟基-4-孕-3-one (20ƒÀ-S)。第二抗体包被到板上,用标记或未标记的20/3-S捕获抗血清。在3小时内,获得了覆盖1.5-192 ƒÊg/井的陡峭标准曲线。该方法的灵敏度和精密度与常规类固醇放射免疫测定法基本相同。这种非同位素分析系统还可以快速测量鲶鱼血浆中的20ƒÀ-S,具有良好的特异性。
A simple solid-phase microtiter plate enzyme-linked immunosorbent assay (ELISA) for 17ƒ¿ , 20ƒÀ, 21-trihydroxy-4-pregnen-3-one (20ƒÀ-S), a teleost maturation inducing steroid, was developed using 20ƒÀ-S-3-CMO-horseradish peroxidase as the label, and a homologous antiserum raised in rabbits. Second antibody coated to the plate was used to capture the antiserum with labeled or unlabeled 20/3-S. Within three hours, a steep standard curve covering 1.5-192 ƒÊg/well was obtained. The sensitivity and precision of this ELISA was almost the same as those of ordinary steroid radioimmunoassays. This non-isotopic assay system also allows prompt measurement of 20ƒÀ-S in catfish plasma with good specificity.