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作 者:朱淮民[1,2] 瞿逢伊[1,2] 刘维德[1,2]
机构地区:[1]第二军医大学寄生虫学教研室 [2]中国科学院上海昆虫研究所
出 处:《中国寄生虫学与寄生虫病杂志》1994年第3期165-168,共4页Chinese Journal of Parasitology and Parasitic Diseases
摘 要:对不同品系致倦库蚊或淡色库蚊分别用抗致倦库蚊酯酶单克隆抗体进行dot-ELISA和夹心法ELISA测定,并与生物测试法和生化微量板法相比较。免疫学检测发现的抗性程度高于后两法,发现的抗性频率高于生化法。ELISA方法诊断抗性的阈值为OD450≥0.5,生化法阈值为β-N浓度≥2.5×10-3μmol/min·mg蛋白。dot-ELISA法适用于现场快速筛选抗性,对高酯酶活力抗性品系的检测优于夹心法ELISA。Different strains of Culex mosquitoes(Cx.pipiens quinquefasciatus and Cx.Pipiens pallens)were immunologically detected for organophosphate resistance with anti esterase monoclonal antibody,and the results were compared with those detected by bioassay and biochemical microplate assay.It was found that the resistance detection rate detected by immunologic methods were higher than the corresponding data detected by the biochemical method,and the levels of resistance detected by sandwich ELISA were higher than the corresponding levels detected by bioassay and the biochemical method.The thresholds for resistance in sandwich ELISA were (at absorbence 450)≥0.5,and in microplate assay were (at absorbence 550)≥2.5×10 3 μmol/min·mg protein. Dot ELISA method was developed to meet the requirement of the field test and proved to be fast and convenient,especially in the detection of samples with higher esterase activity.
分 类 号:R384.1[医药卫生—医学寄生虫学]
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