首页 | 本学科首页   官方微博 | 高级检索  
     检索      

彩鲫ran基因原核表达蛋白多克隆抗体的制备
引用本文:李常健,蒋琼凤.彩鲫ran基因原核表达蛋白多克隆抗体的制备[J].淡水渔业,2006,36(2):3-5.
作者姓名:李常健  蒋琼凤
作者单位:湖南科技学院生命科学与化学工程系,湖南永州,425006
基金项目:湖南省自然科学基金项目(编号:05JJ40035),湖南省高等学校科研经费(青年项目,编号:04B052)资助
摘    要:采用SDS-PAGE分离纯化彩鲫(Carassius auratus gibelio)ran基因编码区cDNA全长序列的原核表达蛋白,并以此为抗原免疫家兔,制备了相应的多克隆抗体;W estern b lotting结果表明,该抗体效价为1∶1000,具有较高的特异性。并从抗原蛋白相对分子质量、每次注射蛋白量、注射方式、注射途径等诸方面对该技术的要点进行了介绍。

关 键 词:彩鲫  ran基因  原核表达蛋白  多克隆抗体
文章编号:1000-6907-(2006)02-0003-03
收稿时间:2005-11-28
修稿时间:2005年11月28

Preparation of Multiclonal Antibody against Expressed Protein of Color Crucian Carp ran Gene in E. Coli
LI Chang-jian,JIANG Qiong-feng.Preparation of Multiclonal Antibody against Expressed Protein of Color Crucian Carp ran Gene in E. Coli[J].Freshwater Fisheries,2006,36(2):3-5.
Authors:LI Chang-jian  JIANG Qiong-feng
Institution:Department of Life Sciences and Chemical Engineering, Hunan Institute of Science and Engineering, Yongzhou, China 425006
Abstract:The protein coded by the full-length cDNA sequence of ran gene from color crucian carp(Carassius auratus gibelio)expressed in E.coli was separated and purified by SDS-PAGE in our study.Moreover,the expressed protein was applied to immunize rabbits and corresponding multiclonal antibody was prepared.Western blotting results indicated that the prepared antibody had the high titer(1∶1000)and high specificity.Moreover,the keys of this technique including the relative molecular mass of antigen,the quantity of proteins in each injection,procedure of injection,and approaches of injection were also introduced in this paper.
Keywords:crucian carp(Carassius auratus gibelio)  ran gene  prokaryotic expression protein  multiclonal antibody
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号