摘要
目的:制备抗人DcR3单克隆抗体(mAb),并鉴定其特异性。方法:纯化的His.DcR3融合蛋白免疫小鼠,应用淋巴细胞杂交瘤技术制备抗人DcR3 mAb并进行纯化,纯化后的抗体经Western blot和ELISA方法鉴定其特异性、Ig亚型和效价。结果:获得5株稳定分泌抗DcR3 mAb的杂交瘤细胞,均属IgG1亚型,其腹水抗体效价为1×10^-5~1×10^-7,Western blot显示5株细胞分泌的mAb均可识别DcR3蛋白,其中1株(181)可与SW480细胞成分反应。结论:成功建立稳定分泌抗人DcR3mAb的杂交瘤细胞株,其分泌的抗体特异性强、效价高,为研究DcR3在组织中的表达、分布及研制ELISA试剂盒奠定基础。
AIM: To prepare monoclonal antibodies (mAbs) against human DcR3 and identify their characterization. METHODS: BALB/c mice were immunized with purified His-DcR3 protein, and mAbs against DcR3 which prepared by hybridoma technique were purified and identified by their specificity, subtype, titers via ELISA and Western blot. RESULTS: Five hybridoma cell lines secreting mAbs against human DcR3 were obtained, which were determined as IgG1 subtype and ascites titers of five mAbs against DcR3 reached 1 × 10^-5 -1 × 10^-7. Five mAbs were proved to recognize His-DcR3 protein specifically, one of which ( 1B1 ) could recognize SW480 cell. CONCLUSION: mAbs against DcR3 with high titers and specificity have been prepared and purified successfully, which laid a foundation for the study of DcR3 expression, distribution in tissu and development of ELISA kit.
出处
《细胞与分子免疫学杂志》
CAS
CSCD
北大核心
2008年第2期139-141,共3页
Chinese Journal of Cellular and Molecular Immunology
基金
国家自然科学基金资助项目(30370617)
吉林省科技发展计划资助项目(20030418-01)