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用于测量大鼠胰岛素的酶联免疫吸附测定(ELISA)与放射免疫测定(RIA)的比较。

Comparison of an enzyme-linked immunosorbent assay (ELISA) with a radioimmunoassay (RIA) for the measurement of rat insulin.

作者信息

Webster H V, Bone A J, Webster K A, Wilkin T J

机构信息

Endocrine Section, Medicine II, Southampton General Hospital, U.K.

出版信息

J Immunol Methods. 1990 Nov 6;134(1):95-100. doi: 10.1016/0022-1759(90)90116-d.

Abstract

A recently developed competitive enzyme-linked immunosorbent assay (ELISA) was compared with a conventional competitive radioimmunoassay (RIA) for the measurement of rat insulin in culture medium. Fifty-six samples were analysed by both assays. There was a correlation coefficient of r = 0.783 between results obtained using the two assay systems. The binding curves of the two assays were differently shaped, so that the ELISA gave good reproducibility over the concentration range 5-50 microU/ml insulin with inter- and intra-assay coefficients of variation less than 14%, but poor reproducibility at higher concentrations. Conversely, the RIA showed excellent reproducibility at concentrations greater than 50 microU/ml insulin, but poor sensitivity and high coefficients of variation below this level. The ELISA procedure offers practical advantages over the RIA, and performs well when measuring physiological concentrations of insulin.

摘要

一种最近开发的竞争性酶联免疫吸附测定法(ELISA)与传统的竞争性放射免疫测定法(RIA)被用于比较测定培养基中的大鼠胰岛素。两种测定法对56个样本进行了分析。使用这两种测定系统获得的结果之间的相关系数r = 0.783。两种测定法的结合曲线形状不同,因此ELISA在胰岛素浓度范围为5 - 50微单位/毫升时具有良好的重复性,批间和批内变异系数小于14%,但在较高浓度时重复性较差。相反,RIA在胰岛素浓度大于50微单位/毫升时显示出优异的重复性,但在此浓度以下灵敏度较差且变异系数较高。ELISA方法相对于RIA具有实际优势,并且在测量生理浓度的胰岛素时表现良好。

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