Beh K J
C.S.I.R.O. Division of Animal Health, McMaster Laboratory, Glebe, N.S.W., Australia.
Vet Immunol Immunopathol. 1988 Feb;18(1):19-27. doi: 10.1016/0165-2427(88)90033-5.
Monoclonal antibodies specific for sheep immunoglobulin light chain, IgM and IgA were produced by conventional cell fusion technology. Purified light chain and IgM were used to verify the specificity of anti-light chain and anti-IgM hybridoma supernatants using passive haemagglutination assays, radioimmunoassays and immunoelectrophoresis. In the absence of pure IgA, verification of monoclonal anti-IgA was, based on paired staining of intestinal lymph smears and comparing the percentage of cells stained with hybridoma supernatant with the percentage of cells stained with polyclonal anti-alpha serum.
通过传统细胞融合技术制备了针对绵羊免疫球蛋白轻链、IgM和IgA的单克隆抗体。使用纯化的轻链和IgM,通过被动血凝试验、放射免疫测定和免疫电泳来验证抗轻链和抗IgM杂交瘤上清液的特异性。由于缺乏纯IgA,基于肠道淋巴涂片的配对染色,并将用杂交瘤上清液染色的细胞百分比与用多克隆抗α血清染色的细胞百分比进行比较,来验证单克隆抗IgA。