中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
An ELISA-like time-resolved fluorescence immunoassay for microcystin detection

文献类型:期刊论文

作者Lei, LM; Wu, YS; Gan, NQ; Song, LR
刊名CLINICA CHIMICA ACTA
出版日期2004-10-01
卷号348期号:1-2页码:177-180
关键词time-resolved fluorescence immunoassay ELISA microcystin
ISSN号0009-8981
通讯作者Song, LR, CAS, Inst Hydrobiol, State Key Freshwater Ecol & Biotechnol, Donghu Nanlu 7, Wuhan 430072, Peoples R China
中文摘要Background: A time-resolved fluorescence immunoassay (TRFIA), based on anti-microcystin-LR (MCLR) monoclonal antibodies (MAbs) and europium-labeled antimouse IgG conjugate, was first developed for microcystin detection. Methods: Anti-MCLR MAbs were prepared by a standard method, and the attained MAbs showed a good cross reactivity with MCLR, MCRR and MCYR. The TRFIA was performed in an indirect competitive mode. The detection method of TRFIA was compared with indirect competitive enzyme-linked immunosorbent assay (ELISA) and high-performance liquid chromatography (HPLC). Results: The TRFIA exhibited a typical sigmoidal response for MCLR at concentrations of 0.005-50 ng/ml, with a wide quantitative range between 0.01 and 10 ng/ml, indicating the broadest detective range and the most sensitive of all the methods for microcystins (MCs) detection. Additionally, the TRFIA maintained good reliability through its quantitative range, as evidenced by low coefficients of variation (1.6-12.2%). The toxin data of algal samples assayed from TRFIA were in the same range as those with ELISA and HPLC, implying that the method was reliable and practical for the detection of MCs. Conclusions: The TRFIA may offer a valuable alternative or a substitute for conventional ELISA for microcystin detection. (C) 2004 Elsevier B.V. All rights reserved.
英文摘要Background: A time-resolved fluorescence immunoassay (TRFIA), based on anti-microcystin-LR (MCLR) monoclonal antibodies (MAbs) and europium-labeled antimouse IgG conjugate, was first developed for microcystin detection. Methods: Anti-MCLR MAbs were prepared by a standard method, and the attained MAbs showed a good cross reactivity with MCLR, MCRR and MCYR. The TRFIA was performed in an indirect competitive mode. The detection method of TRFIA was compared with indirect competitive enzyme-linked immunosorbent assay (ELISA) and high-performance liquid chromatography (HPLC). Results: The TRFIA exhibited a typical sigmoidal response for MCLR at concentrations of 0.005-50 ng/ml, with a wide quantitative range between 0.01 and 10 ng/ml, indicating the broadest detective range and the most sensitive of all the methods for microcystins (MCs) detection. Additionally, the TRFIA maintained good reliability through its quantitative range, as evidenced by low coefficients of variation (1.6-12.2%). The toxin data of algal samples assayed from TRFIA were in the same range as those with ELISA and HPLC, implying that the method was reliable and practical for the detection of MCs. Conclusions: The TRFIA may offer a valuable alternative or a substitute for conventional ELISA for microcystin detection. (C) 2004 Elsevier B.V. All rights reserved.
WOS标题词Science & Technology ; Life Sciences & Biomedicine
学科主题Medical Laboratory Technology
类目[WOS]Medical Laboratory Technology
研究领域[WOS]Medical Laboratory Technology
关键词[WOS]CYANOBACTERIAL TOXINS
收录类别SCI
语种英语
WOS记录号WOS:000224337100024
公开日期2010-10-13
源URL[http://ir.ihb.ac.cn/handle/152342/9406]  
专题水生生物研究所_中科院水生所知识产出(2009年前)_期刊论文
作者单位1.CAS, Inst Hydrobiol, State Key Freshwater Ecol & Biotechnol, Wuhan 430072, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
推荐引用方式
GB/T 7714
Lei, LM,Wu, YS,Gan, NQ,et al. An ELISA-like time-resolved fluorescence immunoassay for microcystin detection[J]. CLINICA CHIMICA ACTA,2004,348(1-2):177-180.
APA Lei, LM,Wu, YS,Gan, NQ,&Song, LR.(2004).An ELISA-like time-resolved fluorescence immunoassay for microcystin detection.CLINICA CHIMICA ACTA,348(1-2),177-180.
MLA Lei, LM,et al."An ELISA-like time-resolved fluorescence immunoassay for microcystin detection".CLINICA CHIMICA ACTA 348.1-2(2004):177-180.

入库方式: OAI收割

来源:水生生物研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。