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一种用于尿液中人白蛋白的竞争性微量滴定板酶免疫测定法的开发与验证。

The development and validation of a competitive, microtiter plate enzymeimmunoassay for human albumin in urine.

作者信息

Akman S, Kurt I, Gultepe M, Dibirdik I, Kilinc C, Kutluay T, Karaca L, Bingol N K

机构信息

Department of Biochemistry, School of Medicine, Gulhane Military Medical Academy, Ankara, Turkey.

出版信息

J Immunoassay. 1995 Aug;16(3):279-96. doi: 10.1080/15321819508013563.

Abstract

We have described a fast, simple and sensitive microtiter scale, solid phase, competitive enzymeimmunoassay (EIA) for the determination of urinary albumin. The albumin used in the test system was purified by the combination of PEG precipitation and DEAE-cellulose column chromatography. In this EIA, microtiter plates were coated with rabbit antihuman albumin IgG, and incubated with HRP-albumin conjugate with either sample or standards. O-phenylenediamine (OPD) and H2O2 solution was used as substrate for HRP. Results obtained correlate well (r = 0.994) with those of an in-house RIA in which same antibody and standards were used as in EIA. The present assay covers the range of 0.5 to 10 mg/L and can be performed in 2 hours. The detection limit was 0.15 mg/L of albumin. Within-assay coefficient of variation was 8.1% and 6.6% and between-assay variation was 10.6% and 8.6% at 1.25 and 2.5 mg/L respectively.

摘要

我们描述了一种用于测定尿白蛋白的快速、简单且灵敏的微量滴定板规模的固相竞争性酶免疫测定法(EIA)。测试系统中使用的白蛋白通过聚乙二醇沉淀和二乙氨基乙基纤维素柱色谱法相结合进行纯化。在这种EIA中,微量滴定板用兔抗人白蛋白IgG包被,并与HRP-白蛋白缀合物与样品或标准品一起孵育。邻苯二胺(OPD)和过氧化氢溶液用作HRP的底物。所得结果与内部放射免疫测定法(RIA)的结果相关性良好(r = 0.994),其中在EIA中使用了相同的抗体和标准品。本测定法涵盖0.5至10 mg/L的范围,可在2小时内完成。白蛋白的检测限为0.15 mg/L。在1.25和2.5 mg/L时,批内变异系数分别为8.1%和6.6%,批间变异为10.6%和8.6%。

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