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牛IFN-γ原核表达、单克隆抗体制备及其ELISA检测方法的建立
引用本文:李川,谭亚娣,陈颖钰,胡巧云,马艳,张桂荣,钦博,晁彦杰,陈焕春,郭爱珍.牛IFN-γ原核表达、单克隆抗体制备及其ELISA检测方法的建立[J].生物工程学报,2007,23(1):40-45.
作者姓名:李川  谭亚娣  陈颖钰  胡巧云  马艳  张桂荣  钦博  晁彦杰  陈焕春  郭爱珍
作者单位:1. 华中农业大学农业微生物学国家重点实验室,武汉,430070
2. 华中农业大学农业微生物学国家重点实验室,武汉,430070;华中农业大学动物医学院预防兽医学省重点实验室,武汉,430070
基金项目:湖北省武汉市科技攻关项目;国家科技攻关项目
摘    要:实验旨在建立牛重组IFN-γ(BovIFN-γ)的ELISA检测技术,为牛传染病的免疫学诊断提供新方法。PHA刺激体外培养的奶牛外周血白细胞,从培养细胞中提取总RNA,经过RT-PCR扩增出BovIFN-γ基因cDNA,进一步克隆至pET28a,转化大肠杆菌,经IPTG诱导,表达出预期大小(18kD左右)组氨酸标记蛋白,经鉴定为BovIFN-γ;以纯化的重组BovIFN-γ为免疫原,应用淋巴细胞杂交瘤技术,获得4株能稳定分泌抗BovIFN-γ单克隆抗体的细胞株,分别命名为A7、A10、G6与G10。免疫球蛋白亚类鉴定证明杂交瘤细胞所分泌的抗体均为IgG1,腹水效价在1∶210×100~1∶211×100之间。Western-blot分析显示,4株单抗均能特异性结合重组BovIFN-γ。ELISA试验表明,4株单抗只与融合蛋白BovIFN-γ反应,而不与非相关性蛋白Ag85B、ESAT-6-CFP-10、GM-CSF等发生反应。选取A10细胞株分泌的单克隆抗体、纯化的多克隆抗体及辣根过氧化物酶(HRP)标记的羊抗兔IgG,建立了检测BovIFN-γ的双抗体夹心ELISA方法。实验结果表明,此方法检测敏感性达到2ng/mL,特异性良好,为进一步建立灵敏、特异的病原感染诊断方法奠定了基础。

关 键 词:牛IFN-γ  单克隆抗体  克隆  表达
文章编号:1000-3061(2007)01-0040-06
修稿时间:7/3/2006 12:00:00 AM

Preparation of Monoclonal Antibodies Against Recombinant Bovine IFN-gamma and Development of Sandwich ELISA for Bovine IFN-gamma Detection
LI Chuan,TAN Ya-Di,CHEN Ying-Yu,HU Qiao-Yun,MA Yan,ZHANG Gui-Rong,QIN Bo,CHAO Yan-Jie,CHEN Huan-Chun and GUO Ai-Zhen.Preparation of Monoclonal Antibodies Against Recombinant Bovine IFN-gamma and Development of Sandwich ELISA for Bovine IFN-gamma Detection[J].Chinese Journal of Biotechnology,2007,23(1):40-45.
Authors:LI Chuan  TAN Ya-Di  CHEN Ying-Yu  HU Qiao-Yun  MA Yan  ZHANG Gui-Rong  QIN Bo  CHAO Yan-Jie  CHEN Huan-Chun and GUO Ai-Zhen
Institution:Key Laboratory of Systematic Mycology and Lichenology; Institute of Microbiology; Chinese Academy of Sciences; Beijing 100080;Key Laboratory of Systematic Mycology and Lichenology; Institute of Microbiology; Chinese Academy of Sciences; Beijing 100080
Abstract:The phylogenetic position of the lichen family Umbilicariaceae is investigated using nucleotide sequences of the nuclear SSU rDNA region. Sequences of 6 species were obtained in this study and aligned to those of other lichenized and non-lichenized fungal species from GenBank. The result indicates that the Umbilicariaceae cannot be included in the order Lecanorales and the order Umbilicariales is supported by both the molecular and morphological data. The new order Umbilicariales within Lecanoromycetes, Ascomycota is described in this paper accordingly.
Keywords:ELISA
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