Horseradish peroxidase (HRP) is generally used as a label enzyme in enzyme immunoassay (EIA).The procedure used for HRP detection in EIA is critical for sensitivity and precision.This paper describes a novel fluorimet...Horseradish peroxidase (HRP) is generally used as a label enzyme in enzyme immunoassay (EIA).The procedure used for HRP detection in EIA is critical for sensitivity and precision.This paper describes a novel fluorimetric assay for horseradish peroxidase (HRP) using sesamol as substrate.The principle of the assay is as follow:sesamol (3,4-methylenedioxy phenol) is reacted enzymatically in the presence of hydrogen peroxide to produce dimeric sesamol.The dimer is fluorescent and can be detected sensitively at ex.347 nm,em.427 nm.The measurable range of HRP was 1.0×10-18 to 1.0×10-15 mol/assay,with a detection limit of 1.0×10-18 mol/assay.The coefficient of variation (CV,n=8) was examined at each point on the standard curve,with a mean CV percentage of 3.8%.This assay system was applied to thyroid stimulating hormone (TSH) EIA using HRP as the label enzyme.展开更多
酶联免疫法(enzyme immunoassay method,EIA)作为一种二口恶英物质的半定量筛选方法被越来越多的实验室使用。与经典的高分辩气相色谱-高分辨质谱法(high-resolution gas chromatrography coupled with high-resolution mass spectromet...酶联免疫法(enzyme immunoassay method,EIA)作为一种二口恶英物质的半定量筛选方法被越来越多的实验室使用。与经典的高分辩气相色谱-高分辨质谱法(high-resolution gas chromatrography coupled with high-resolution mass spectrometry,HRGC-HRMS)不同,ELISA方法得到检测样本总二口恶英类物质的含量,两种方法之间存在偏差。文章引入校正调节因子(calibration adjustment factor,CAF)来减少这种偏差。通过对本实验室前期工作中得到的47组土壤样品二口恶英数据进行统计分析,计算得到土壤来源二口恶英EIA检测方法的校正调节因子为0.6。后期实验室进行崇明岛土壤二口恶英水平研究时,对得到的土壤样品EIA检测结果使用本文得到的CAF值进行校正,验证CAF值的作用。校正前,两组数据之间存在显著性差异,校正后,数据相近,且无显著性差异。证明此CAF值在土壤样品中的适用性。展开更多
文摘Horseradish peroxidase (HRP) is generally used as a label enzyme in enzyme immunoassay (EIA).The procedure used for HRP detection in EIA is critical for sensitivity and precision.This paper describes a novel fluorimetric assay for horseradish peroxidase (HRP) using sesamol as substrate.The principle of the assay is as follow:sesamol (3,4-methylenedioxy phenol) is reacted enzymatically in the presence of hydrogen peroxide to produce dimeric sesamol.The dimer is fluorescent and can be detected sensitively at ex.347 nm,em.427 nm.The measurable range of HRP was 1.0×10-18 to 1.0×10-15 mol/assay,with a detection limit of 1.0×10-18 mol/assay.The coefficient of variation (CV,n=8) was examined at each point on the standard curve,with a mean CV percentage of 3.8%.This assay system was applied to thyroid stimulating hormone (TSH) EIA using HRP as the label enzyme.
文摘酶联免疫法(enzyme immunoassay method,EIA)作为一种二口恶英物质的半定量筛选方法被越来越多的实验室使用。与经典的高分辩气相色谱-高分辨质谱法(high-resolution gas chromatrography coupled with high-resolution mass spectrometry,HRGC-HRMS)不同,ELISA方法得到检测样本总二口恶英类物质的含量,两种方法之间存在偏差。文章引入校正调节因子(calibration adjustment factor,CAF)来减少这种偏差。通过对本实验室前期工作中得到的47组土壤样品二口恶英数据进行统计分析,计算得到土壤来源二口恶英EIA检测方法的校正调节因子为0.6。后期实验室进行崇明岛土壤二口恶英水平研究时,对得到的土壤样品EIA检测结果使用本文得到的CAF值进行校正,验证CAF值的作用。校正前,两组数据之间存在显著性差异,校正后,数据相近,且无显著性差异。证明此CAF值在土壤样品中的适用性。
