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[孕酮的偏振荧光免疫测定法]

[Polarization fluoroimmunoassay of progesterone].

作者信息

Kolosova A Iu, Eremin S A, Gavrilova E M, Egorov A M

出版信息

Probl Endokrinol (Mosk). 1994 Jul-Aug;40(4):48-51.

PMID:7971912
Abstract

A quick reliable homogeneous polarization fluoroimmunoassay (PFIA) of progesterone was developed. The assay is carried out with Abbott TDx (USA) polarization fluorometer and it takes 5-7 min to analyze 10 samples by this method. The range of progesterone concentrations determined is 1 to 1000 ng/ml. Fluorescein labeled progesterone-3-carboxymethyloxime which was used as tracer (labeled antigen) during analysis has been synthesized and purified. Two types of PFIA were developed: one making use of rabbit antiserum to progesterone-3-carboxymethyloxime conjugated with bovine serum albumin (BSA) or keyhole limpet hemocyanin (KLH), in the other antiserum to progesterone-11-hemisuccinate-BSA (or KLH) is used. Different combinations of the tracer and antibodies were used. The sensitivity of heterologous PFIA (with antibodies to immunogen heterologous to tracer by structure) was higher than that of homologous PFIA. The test is sufficiently sensitive and specific. The method is particularly valuable for determination of progesterone in model solutions (using buffer standards).

摘要

建立了一种快速可靠的孕酮均相偏振荧光免疫分析方法(PFIA)。该分析使用美国雅培TDx偏振荧光计进行,用此方法分析10个样品需要5 - 7分钟。所测定的孕酮浓度范围为1至1000 ng/ml。分析过程中用作示踪剂(标记抗原)的荧光素标记孕酮 - 3 - 羧甲基肟已合成并纯化。开发了两种类型的PFIA:一种使用兔抗孕酮 - 3 - 羧甲基肟与牛血清白蛋白(BSA)或钥孔戚血蓝蛋白(KLH)偶联的抗血清,另一种使用抗孕酮 - 11 - 半琥珀酸 - BSA(或KLH)抗血清。使用了示踪剂和抗体的不同组合。异源PFIA(使用针对结构上与示踪剂异源的免疫原的抗体)的灵敏度高于同源PFIA。该检测具有足够的灵敏度和特异性。该方法对于测定模型溶液(使用缓冲标准品)中的孕酮特别有价值。

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