Silberman L G, Datta N, Hoops P, Roux S J
Arch Biochem Biophys. 1985 Jan;236(1):150-8. doi: 10.1016/0003-9861(85)90614-9.
A library of 50 hybridomas which make antibodies to oat phytochrome was produced from the fusion of spleen cells from immunized Balb/c mice with P3x63Ag8 myeloma cells. Hybridomas were selected in a medium containing hypoxanthine, aminopterin, and thymidine, and specific hybridomas were screened for production of antibodies to phytochrome using a solid-phase enzyme-linked immunoadsorbent assay which was antigen specific. Positive cultures were cloned three times by limit dilution to assure monoclonal growth and stability. Specificity toward phytochrome was established by Western blot analysis and immunoprecipitation. Epitope specificity of nine monoclonal antibodies was determined by competitive inhibition radioimmunoassays and/or comparative immunoblots of tryptic peptides of phytochrome.
通过将免疫后的Balb/c小鼠的脾细胞与P3x63Ag8骨髓瘤细胞融合,产生了一个包含50种能产生燕麦光敏色素抗体的杂交瘤文库。杂交瘤在含有次黄嘌呤、氨基蝶呤和胸腺嘧啶核苷的培养基中进行筛选,使用抗原特异性的固相酶联免疫吸附测定法筛选产生光敏色素抗体的特定杂交瘤。阳性培养物通过有限稀释法克隆三次,以确保单克隆生长和稳定性。通过蛋白质印迹分析和免疫沉淀确定对光敏色素的特异性。通过竞争性抑制放射免疫测定和/或光敏色素胰蛋白酶肽段的比较免疫印迹确定9种单克隆抗体的表位特异性。