Ginel P J, Margarito J M, Molleda J M, López R, Novales M, Bernadina W E
Department of Clinical Pathology, University of Córdoba Faculty of Veterinary Medicine, Spain.
Res Vet Sci. 1996 Mar;60(2):107-10. doi: 10.1016/s0034-5288(96)90002-8.
An amplified capture enzyme-linked immunosorbent assay (ELISA) has been developed by the use of the biotin-avidin detection system, for the measurement of canine plasma immunoglobulins (Ig) A, G and M. Test responses of dilutions of both the Ig standards and test plasma samples were consistently linear (r > 0.987) for the three Ig classes. The within-assay variation was 3.53 per cent for IgG, 5.84 per cent for IgM and 6.34 per cent for IgA. The analytical recoveries were 95 per cent for IgA, 97 per cent for IgG and 98 per cent for IgM. The lower detection limits of the assay were 38.4 ng ml-1 for IgG, 20.3 ng ml-1 for IgM and 41.2 ng ml-1 for IgA. The results indicate that this ELISA has a much higher sensitivity than the single radial immunodiffusion assay or the non-amplified ELISA for measurements of canine Igs, but has a comparable specificity and precision.
利用生物素-抗生物素蛋白检测系统开发了一种扩增捕获酶联免疫吸附测定(ELISA)法,用于测定犬血浆免疫球蛋白(Ig)A、G和M。三种Ig类别的Ig标准品和测试血浆样品稀释液的测试反应均呈一致的线性(r>0.987)。该检测方法的批内变异系数为:IgG为3.53%,IgM为5.84%,IgA为6.34%。分析回收率为:IgA为95%,IgG为97%,IgM为98%。该检测方法的最低检测限为:IgG为38.4 ng/ml-1,IgM为20.3 ng/ml-1,IgA为41.2 ng/ml-1。结果表明,与单扩散免疫比浊法或未扩增的ELISA法相比,该ELISA法在测定犬Ig时具有更高的灵敏度,但特异性和精密度相当。