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高香草酸-H_2O_2-HRP荧光酶联免疫分析测定HRP的研究
引用本文:张书圣,焦奎,季先锋.高香草酸-H_2O_2-HRP荧光酶联免疫分析测定HRP的研究[J].青岛科技大学学报,1997(4).
作者姓名:张书圣  焦奎  季先锋
作者单位:青岛化工学院应用化学系!青岛266042
基金项目:青岛化工学院青年科学基金
摘    要:提出了高香草酸-H2O2-HRP荧光酶联免疫分析测定HRP的新方法。该法基于HRP催化H2O2氧化高香草酸生成能产生荧光的物质,该物质在Ex=317nm激发光作用下产生荧光,通过测定在Em=421nm处的荧光强度,间接测定HRP的含量。在所选定的实验条件下,对HRP测定线性范围为1.0×10(-10)~1.0×10(-8)g/mL,检测限为1.0×10(-10)g/mL。

关 键 词:荧光光度法  免疫分析  辣根过氧化物酶  高香草酸

Fluorescence Enzyme Linked Immunoassay to Detect HRP Using Homovanillic- H_2O_2-HRP System
Zhang Shusheng, Jiao Kui ,Ji Xianfeng.Fluorescence Enzyme Linked Immunoassay to Detect HRP Using Homovanillic- H_2O_2-HRP System[J].Journal of Qingdao University of Science and Technology:Natutral Science Edition,1997(4).
Authors:Zhang Shusheng  Jiao Kui  Ji Xianfeng
Abstract:A new system for the determination of horse radish peroxidase (HRP) was investigated by fluorescence enzyme linked immunoassay. H2O2 could oxidate homovanillic acid catalyzed by HRP to produce a substance which emitted fluorescence (Ex=317nm, Em=421nm), and so HRP could be detected by measuring the density of fluorescence of the oxidaited product. The linear range of the method to detect HRP is (1.0×10(-10)~ 1.0×10(-8)g/mL,and the detection limit 1.0×10(-10)g/mL.
Keywords:fluorescence spectrophotometry  enzyme  immunoassay  horse radish peroxidase  homovanillic  
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