检测猴艾滋病D型逆转录病毒抗体的ELISA技术

云南省应用基础研究基盎以及云南夏长娄中心和昆明动物所 长羹生物学旺台实验室基金资助。

定量ELISA检测小鼠血清中抗LDH-C4IgG2b抗体的水平

用定量EL ISA 的方法检测背部携带分泌抗LDH - C4 IgG2b 抗体杂交瘤小鼠的血清中IgG2b 抗体浓 度, 结果表明: 本法稳定, 批间变异系数为7104 %～13130 % , 批内变异系数为3161 %～10120 %; 标准曲线 相关性良好, 相关系数从01962 884～01996 795 ; 灵敏度较高, 最低检出浓度为0101 mg/ L ; 特异性亦较好.

圆形碘孢虫完整孢子ELISA的建立

探索建立鱼类寄生圆形碘孢虫(MyxobolusrotundusNemezek,1911,Myxosporea,Bivalvulida)完整孢子酶联免疫吸附试验(Enzyme linkedimmunosorbentassay,ELISA)检测的可行性,对丙酮、戊二醛、甲醛、多聚甲醛、乙醇等几种常用固定剂应用于此方法的效果进行评价,初步建立了针对鱼类黏孢子虫的完整孢子ELISA检测模式。结果显示,同比其他几种固定剂,2%的多聚甲醛、0 25%的戊二醛对圆形碘孢虫完整孢子ELISA有较好的效果,经二者固定后,最

An ELISA-like time-resolved fluorescence immunoassay for microcystin detection

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.