Anderson S J, Furth M E, Wolff L, Ruscetti S K, Sherr C J
J Cell Biochem. 1982;19(3):275-80. doi: 10.1002/jcb.240190309.
The McDonough strain of feline sarcoma virus (SM-FeSV) contains a viral oncogene, v-fms, transduced from cat cellular genetic sequences designated c-fms. Monoclonal antibodies reactive to antigenic determinants encoded by v-fms were prepared by immunizing rats with live, syngeneic SM-FeSV-transformed cells, and fusing splenic lymphocytes from a tumor-bearing animal with cultured rat myeloma cells. Culture supernatants from hybrids producing antibodies to epitopes encoded by v-fms were identified by immunoprecipitation of radiolabeled polypeptides from SM-FeSV-transformed mink cells. Four positive hybrids were cloned twice in soft agar, established as stable lines, and grown in defined serum-free medium to facilitate purification of homogeneous antibodies. The monoclonal antibodies were used to assay SM-FeSV-specific products by "immunoblotting" of electrophoretically separated proteins, and by fixed-cell immunofluorescence.
猫肉瘤病毒的麦克多诺毒株(SM-FeSV)含有一个从猫细胞遗传序列(称为c-fms)转导而来的病毒癌基因v-fms。通过用同基因的活SM-FeSV转化细胞免疫大鼠,并将荷瘤动物的脾淋巴细胞与培养的大鼠骨髓瘤细胞融合,制备了对v-fms编码的抗原决定簇有反应的单克隆抗体。通过对SM-FeSV转化的貂细胞中的放射性标记多肽进行免疫沉淀,鉴定产生针对v-fms编码表位抗体的杂交瘤培养上清液。四个阳性杂交瘤在软琼脂中克隆两次,建立稳定细胞系,并在限定的无血清培养基中培养,以利于纯化同质抗体。这些单克隆抗体通过对电泳分离的蛋白质进行“免疫印迹”以及固定细胞免疫荧光来检测SM-FeSV特异性产物。