Slappendel R J, Frielink R A, Mol J A, Noordzij A, Hamer R
Department of Clinical Sciences of Companion Animals, Medical Faculty, University of Utrecht, Netherlands.
Vet Immunol Immunopathol. 1992 Jun;33(1-2):145-54. doi: 10.1016/0165-2427(92)90041-n.
A quantitative enzyme-linked immunosorbent assay (ELISA) has been developed to measure canine von Willebrand factor antigen (vWf-Ag) in plasma of the dog. A vWf-Ag antiserum was raised in rabbits and purified by preabsorption with the low molecular weight vWf-Ag-deficient fraction of canine cryoprecipitate, followed by affinity chromatography on protein-A Sepharose. The rabbit anticanine vWf-Ag IgG was used to bind the vWf-Ag of the test plasmas to the solid phase and to prepare the enzyme-antibody conjugate in ELISA. Normal rat serum was used as blocking agent. The standard curve was linear (r2 greater than 0.98) and reproducible after logit-log transformation. The interassay coefficient of variation (CV) in test plasmas with various vWf-Ag concentrations was never greater than 7.7%. Assayed values in dilutions of pooled normal canine plasma added to canine vWf-Ag-deficient plasma were linear between 0 and 100% (r2 = 0.99) and indicated excellent analytical recovery of vWf-Ag. In 18 dogs with various internal diseases, including von Willebrand's disease and haemophilia A, the coefficient of correlation between the results of the ELISA and those of electroimmunodiffusion (EID) was 0.93.
已开发出一种定量酶联免疫吸附测定法(ELISA)来测量犬血浆中的犬血管性血友病因子抗原(vWf-Ag)。用犬冷沉淀中低分子量vWf-Ag缺陷部分对兔进行预吸收,然后在蛋白A琼脂糖凝胶上进行亲和层析,从而制备并纯化了vWf-Ag抗血清。在ELISA中,兔抗犬vWf-Ag IgG用于将测试血浆中的vWf-Ag结合到固相上,并制备酶-抗体偶联物。使用正常大鼠血清作为封闭剂。经对数-对数转换后,标准曲线呈线性(r2大于0.98)且具有可重复性。不同vWf-Ag浓度的测试血浆中的批间变异系数(CV)从未超过7.7%。添加到犬vWf-Ag缺陷血浆中的混合正常犬血浆稀释液中的测定值在0至100%之间呈线性(r2 = 0.99),表明vWf-Ag具有出色的分析回收率。在18只患有包括血管性血友病和A型血友病在内的各种内科疾病的犬中,ELISA结果与免疫电泳(EID)结果之间的相关系数为0.93。