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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Time-resolved fluoroimmunoassay for unconjugated estrogen in urine: comparison with a fluorometric assay for total estrogen and application in an in vitro fertilization program.
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Time-resolved fluoroimmunoassay for unconjugated estrogen in urine: comparison with a fluorometric assay for total estrogen and application in an in vitro fertilization program.

机译:尿液中未结合的雌激素的时间分辨荧光免疫测定:与总雌激素的荧光测定比较,并在体外受精程序中应用。

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A time-resolved fluoroimmunoassay (TR-FIA) for unconjugated estrogens in human urine is described. 6-Keto-17 beta-estradiol-6-(O-carboxymethyl)oxime:bovine serum albumin is immobilized onto microtiter strip wells and the coated wells are incubated with 17 beta-estradiol standard preparations or unknowns with a polyclonal antiserum to 17 beta-estradiol-16,17-monosuccinyl:albumin. The antiserum-bound estrogen is detected by incubation with a europium-labeled anti-rabbit IgG that serves as both second antibody and tracer. After the immunoreactions, the bound portion of the labeled antiserum is quantified by dissociating the Eu3+ in a fluorescence-enhancement solution and measuring its fluorescence with a time-resolved fluorometer. The detection limit of the TR-FIA is 24 pmol of 17 beta-estradiol per liter; the analytical range extends to 1.8 nmol/L. This assay is a convenient alternative to radioimmunoassay and to the automated Kober-Ittrich fluorometry of total estrogen. Its advantages include short counting times; use of nonradioactive, stable reagents, all of which are commercially available; and more nearly complete automation. We conclude that this TR-FIA, compared with the Kober-Ittrich fluorometric assay (J Endocrinol 1957; 16:49-56), provides the clinician with equivalent information during follicular development therapy as part of an in vitro fertilization program.
机译:描述了一种用于人类尿液中未结合雌激素的时间分辨荧光免疫测定法(TR-FIA)。将6-酮-17β-雌二醇-6-(O-羧甲基)肟:牛血清白蛋白固定在微量滴定条孔上,然后将包被的孔与17种β-雌二醇标准制剂或未知物一起用多克隆抗血清温育至17β-雌二醇-16,17-单琥珀酰:白蛋白。通过与用作第二抗体和示踪剂的euro标记的抗兔IgG孵育来检测抗血清结合的雌激素。免疫反应后,通过在荧光增强溶液中解离Eu3 +并用时间分辨荧光计测量其荧光来定量标记抗血清的结合部分。 TR-FIA的检出限为每升24 pmol 17β-雌二醇。分析范围扩展到1.8 nmol / L。该测定法是放射免疫测定法和总雌激素自动Kober-Ittrich荧光测定法的简便替代方法。它的优点包括计数时间短;使用非放射性,稳定的试剂,所有试剂均可商购;以及几乎完全的自动化。我们得出的结论是,与Kober-Ittrich荧光测定法(J Endocrinol 1957; 16:49-56)相比,这种TR-FIA作为体外受精程序的一部分,为卵泡发育治疗期间的临床医生提供了等效信息。

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