Kelley K W, Kleiss A J, Brief S
Department of Animal Sciences, University of Illinois, Urbana 61801.
Am J Vet Res. 1988 Jun;49(6):944-9.
Using radioimmunoassay methods, quality control criteria were applied to monoclonal antibodies produced to measure porcine immunoglobulins by quantitative ELISA. Porcine IgM and IgA were purified to homogeneity and were used to produce murine hybridomas that secreted antibodies against IgM, IgA, and immunoglobulin light chains. A competitive ELISA was developed to measure IgM, and a sandwich ELISA was used to quantify IgA in serum and colostrum. Both ELISA were tested for specificity, accuracy, sensitivity, and precision. Monoclonal antibodies were specific for porcine IgM or IgA in serum and colostrum, and competitive and sandwich ELISA fulfilled all validation criteria.
采用放射免疫分析方法,将质量控制标准应用于通过定量酶联免疫吸附测定(ELISA)检测猪免疫球蛋白所产生的单克隆抗体。猪IgM和IgA被纯化至同质,并用于制备分泌抗IgM、IgA和免疫球蛋白轻链抗体的小鼠杂交瘤。开发了一种竞争性ELISA来检测IgM,并使用夹心ELISA对血清和初乳中的IgA进行定量。对这两种ELISA均进行了特异性、准确性、敏感性和精密度测试。单克隆抗体对血清和初乳中的猪IgM或IgA具有特异性,竞争性ELISA和夹心ELISA均符合所有验证标准。