当前位置: 首页 > 期刊 > 《细胞与分子免疫学杂志》 > 2007年第3期
编号:11410657
抗MDV1 VP22羧基端单克隆抗体的制备与免疫学特性鉴定
http://www.100md.com 《细胞与分子免疫学杂志》 2007年第3期
马立克氏病病毒;,VP22,羧基端;,单克隆抗体;,特性鉴定,,]马立克氏病病毒;,VP22,羧基端;,单克隆抗体;,特性鉴定,抗MDV1VP22羧基端单克隆抗体的制备与免疫学特性鉴定,1材料和方法,2结果,3讨论,参考文献:
     Preparation and immunological characterization of monoclonal antibodies against VP22 carboxyl terminus of Marek’s disease virus serotype 1

    SONG Cuiping, CHEN Hongjun, QIN Aijian*, ZHANG Chenfei

    Key Lab of Jiangsu Preventive Veterinary Medicine, College of Veterinary Medcine, Yangzhou University, Yangzhou 225009, China

    [Abstract] AIM: To prepare and characterize monoclonal antibodies (mAb) against VP22 carboxyl terminus of CVI988/Rispens strain of Marek’s disease virus serotype 1. METHODS: Carboxyl terminus of CVI988 VP22 (94aa~243aa) was expressed in prokaryotic system. mAbs against VP22 were prepared by hybridoma technology from BALB/c mice immunized with the fusion protein GSTVP22C and characterized by ELISA, indirect fluorescence assay (IFA) and Western blot. RESULTS: Two hybridoma cell lines stably secreting mAb against VP22C were obtained and designated as 3F7 and 4E4. mAb 3F7 could react with VP22 expressed in all the plaques, while mAb 4E4 stained all the cells nuclei in MDVinfected CEF cells. It was also found that 3F7 could react with VP22 expressed in Sf9 cells and denatured VP22 by Western blot analysis. In addition, it was further showed that the epitope of mAb 3F7 was located within the domain between 94aa and 193aa, the predicted site of protein transduction domain of VP22. CONCLUSION: The preparation of the mAb is very important to further research in protein transduction domain of MDV1 VP22. ......

您现在查看是摘要页,全文长 12774 字符