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使用单克隆抗体的胰岛素一步夹心酶免疫测定法。

One-step sandwich enzyme immunoassay for insulin using monoclonal antibodies.

作者信息

Bürgi W, Briner M, Franken N, Kessler A C

机构信息

Department of Laboratory Medicine, Kantonsspital Aarau, Switzerland.

出版信息

Clin Biochem. 1988 Oct;21(5):311-4. doi: 10.1016/s0009-9120(88)80087-0.

Abstract

An enzyme-linked immunosorbent assay for the measurement of insulin in human serum has been developed. The test is based on the sandwich technique with two monoclonal antibodies directed against two different epitopes of insulin using coated plastic tubes as the solid phase and horse radish peroxidase as the label. The immunoreactions are completed in one step within 2 h. The horse radish peroxidase activity bound to the tube wall is measured photometrically after an additional 1-h incubation with the substrate. The standards used cover the range from 0 to 260 mU insulin/L. Employing the Enzymun-Test System ES 22 modular batch analyzer, the detection limit was found to be 3.7 mU insulin/L. Coefficients of variation (CV's) between 1.4-7.8% for intraassay precision and 5.6-10% for interassay precision were obtained over the concentration range of 17-107 mU Insulin/L. The correlation between the procedure described here (y) and a commercially available double antibody radioimmunoassay (x) is expressed by the following equation: y = 1.07x + 1.14 mU insulin/L.

摘要

已开发出一种用于测定人血清中胰岛素的酶联免疫吸附测定法。该测试基于夹心技术,使用针对胰岛素两个不同表位的两种单克隆抗体,以包被的塑料管作为固相,辣根过氧化物酶作为标记物。免疫反应在2小时内一步完成。在与底物额外孵育1小时后,通过光度法测量与管壁结合的辣根过氧化物酶活性。所用标准品涵盖0至260 mU胰岛素/L的范围。使用酶免疫检测系统ES 22模块化批量分析仪,检测限为3.7 mU胰岛素/L。在17 - 107 mU胰岛素/L的浓度范围内,批内精密度的变异系数(CV)为1.4 - 7.8%,批间精密度的变异系数为5.6 - 10%。此处所述方法(y)与市售双抗体放射免疫测定法(x)之间的相关性由以下方程表示:y = 1.07x + 1.14 mU胰岛素/L。

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