GONG Zhen-li, LIU Xiang-tao, TIAN Hong, WU Jin-yan, DAI Xing-guo, SHANG You-jun and CHEN Guo-dong. Expression of FMDV P1+2A Gene in BHK-21 Cells[J]. Virologica Sinica, 2006, 21(5): 454-457.
Citation: GONG Zhen-li, LIU Xiang-tao, TIAN Hong, WU Jin-yan, DAI Xing-guo, SHANG You-jun, CHEN Guo-dong. Expression of FMDV P1+2A Gene in BHK-21 Cells .VIROLOGICA SINICA, 2006, 21(5) : 454-457.

口蹄疫病毒P1+2A基因在BHK-21细胞中的表达

  • 本研究将已构建好的、包含口蹄疫病毒P1+2A基因的重组表达质粒pQE-Tri/P1+2A经质脂体2000转染哺乳动物细胞BHK-21,转染后一定时间进行检测。通过SDS-PAGE、Western-blotting、荧光抗体染色、ELISA等检测方法表明,FMDV P1+2A基因片段在BHK-21细胞中成功表达,表达的蛋白能被口蹄疫阳性血清所识别而且具有良好的生物学活性。这一结果的取得,为进一步研制新型口蹄疫基因工疫苗及其配套诊断试剂奠定了基础。

Expression of FMDV P1+2A Gene in BHK-21 Cells

  • In this study, recombinant expression plasmid pQE-Tri/P1+2A was constructed and then transfected into BHK-21 cell line mediated by liposome 2000. The results of SDS-PAGE、Western-blotting、fluorescence antibody and ELISA showed that FMDV P1+2A protein was expressed in BHK-21 cell line successfully and can be recognized by FMD positive serum. The result will lay a foundation for study of FMDV gene engineered vaccines as well as the development of diagnostic reagents.

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    Expression of FMDV P1+2A Gene in BHK-21 Cells

    • 1. Key Laboratory of Animal Virology, Ministry of Agriculture Lanzhou Veterinary Research Institute, Lanzhou 730046,China

    Abstract: In this study, recombinant expression plasmid pQE-Tri/P1+2A was constructed and then transfected into BHK-21 cell line mediated by liposome 2000. The results of SDS-PAGE、Western-blotting、fluorescence antibody and ELISA showed that FMDV P1+2A protein was expressed in BHK-21 cell line successfully and can be recognized by FMD positive serum. The result will lay a foundation for study of FMDV gene engineered vaccines as well as the development of diagnostic reagents.

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