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作 者:梅建军[1] 王兴龙[2] 万忠海[2] 李晓燕[2] 马云志[2] 张辉[3] 崔丽瑾[3]
机构地区:[1]内蒙古包头医学院基础医学部,包头014010 [2]军事医学科学院军事兽医研究所,长春130062 [3]吉林大学农学部,长春130062
出 处:《中国生物制品学杂志》2007年第10期771-774,共4页Chinese Journal of Biologicals
摘 要:目的研制羊布鲁菌O链M纯化抗原及其单克隆抗体。方法采用冷酚法提纯羊布鲁菌16M的O链抗原,并经琼脂糖凝胶免疫扩散和SDS-PAGE鉴定,用灭活的该抗原免疫BALB/c小鼠,制备单克隆抗体,并进行鉴定。结果建立3株分泌单克隆抗体的细胞株2D10、3C6和1E10,ELISA效价分别为1.380、1.109和1.048,与大肠杆菌0:157、小肠结肠炎耶尔森菌0:9、鼠伤寒沙门菌和猪胸膜肺炎放线杆菌均无交叉反应。3C6和1E10与牛布鲁菌544A发生交叉反应,2D10的亲和常数达5.30×10~7M^(-1)。结论已制备出纯化的羊布鲁菌O链M抗原及其单抗。Objective To prepare purified B. melitensis 0 chain M antigen and its specific monoclonal antibody(McAb). Methods Purify the O chain from B. melitensis 16M by cold phenol extraction and identify by agarose gel immunodiffusion and SDS-PAGE. Immunize BALB/c mice with inactivated O chain antigen to prepare McAb. Results Three cell strains secreting McAb against O chain antigen, i. e. 2D10,3C6 and 1 El0, were established, and their ELISA titers were 1. 380,1. 109 and 1. 048 respectively. The secreted McAbs showed no cross reaction with E. coli O:157, Y. enterocolitica 0:9 ,S. typhimurium and Actinobaciilus. However, the McAbs secreted by 3C6 and 1El0 showed cross reaction with B. abortus 544A,and the affinity constant of McAb secreted by 2D10 reached 5.30 x 10^7 M^-1. Conclusion Purified B. melitensis 0 chain M and its specific McAb were successfully prepared.
分 类 号:R378.8[医药卫生—病原生物学] R392.33[医药卫生—基础医学]
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