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氨甲酰磷酸合成酶单克隆抗体的制备、鉴定及应用
引用本文:鞠艳芳,刘蓉,杨金菊,柳晓兰,高建恩,孙启鸿. 氨甲酰磷酸合成酶单克隆抗体的制备、鉴定及应用[J]. 细胞与分子免疫学杂志, 2008, 24(5): 479-481
作者姓名:鞠艳芳  刘蓉  杨金菊  柳晓兰  高建恩  孙启鸿
作者单位:1. 解放军总医院肿瘤内科,北京,100853
2. 军事医学科学院放射与辐射医学研究所十二室,北京,100850
3. 北京蛋白质组研究中心,北京,102206
4. 军事医学科学院放射与辐射医学研究所十二室,北京,100850;北京蛋白质组研究中心,北京,102206
基金项目:国家科技攻关项目 , 国家重点基础研究发展计划(973计划)
摘    要:目的:制备抗人氨甲酰磷酸合成酶(CPSI)的单克隆抗体(mAb)并进行初步鉴定与应用.方法:将正常成人肝组织匀浆离心并分离线粒体,用线粒体总蛋白免疫BALB/c小鼠,采用杂交瘤技术制备 mAb,并通过间接ELISA法、Western blot、免疫组化及免疫荧光染色的方法对mAb进行特性鉴定,通过免疫沉淀联合质谱、Uni-ZAP XR表达文库筛选鉴定抗原,借助免疫捕获的方法用抗体来分离复合物.结果:获得3株可稳定分泌抗人CPSI mAb的杂交瘤细胞系.mAb的Ig亚类(型)为IgGl(K),该mAb可用于ELISA检测、Western blot、免疫组化、免疫荧光染色、免疫沉淀实验和复合物的分离.结论:成功制备了抗人CPSI的mAb,为CPSI的研究提供了有力的工具.

关 键 词:氨甲酰磷酸合成酶(CPSI)  单克隆抗体  特性  氨甲酰  磷酸  合成酶  单克隆抗体  应用  Preparation  monoclonal antibody  application  研究  实验  检测  杂交瘤细胞系  稳定  结果  复合物  免疫捕获  抗原  筛选鉴定  表达文库  质谱
文章编号:1007-8738(2008)05-0479-03
修稿时间:2007-12-22

Preparation,characterization and application of monoclonal antibody against CPS1
JU Yan-fang,LIU Rong,YANG Jin-ju,LIU Xiao-lan,GAO Jian-en,SUN Qi-hong. Preparation,characterization and application of monoclonal antibody against CPS1[J]. Chinese journal of cellular and molecular immunology, 2008, 24(5): 479-481
Authors:JU Yan-fang  LIU Rong  YANG Jin-ju  LIU Xiao-lan  GAO Jian-en  SUN Qi-hong
Affiliation:General Hospital of Beijing, Beijing 100853, China.
Abstract:AIM: To prepare and characterize the monoclonal antibody (mAb) against human carbamyl phosphate synthetase I (CPSI) and makea study of its application. METHODS: Normal human liver tissues were homogenized, and their mitochondria were isolated by differential centrifugation. The total mitochondrial proteins were used to immunize BALB/c mice to prepare mAb using the routine hybridoma technique. The mAb was detected by ELISA, Western blot immunohistochemistry and immunofluorecent staining. The specificity of mAb was identified by mass spectrometry (MS) and immunoprecipitation (IP) and then confirmed by Uni-ZAP expression library screening. The antibody was used to isolate potential enzymatic complexes by immunocapturing. RESULTS: Three hybridoma cell lines BEH045, ACB271 and BFG021 secreting specific mAb against CPS1 were obtained. The Ig subclass of the mAb was IgG(1), which was used in ELISA, Western blot immunohistochemistry, immunoprecipitation, immunofluorecent staining and the isolation of potential enzymatic complexes. CONCLUSION: A hybridoma cell line which can secre specific mAb against CPSI stably has been established. The specific mAb against CPSI is of valne to the research into the functions and distribution of CPSI.
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