REN Xue-feng, HU Zhi-hua, TAN Guo-lei, ZHOU Bing, XU Xue-qin, ZHENG Qi-sheng, Zhang Xiao-yong, CHEN De-sheng and CHEN Pu-yan*. Expression of the Domain Gene of Porcine Parvovirus VP2 with the Eukaryotic Vector pIREShyg*[J]. Virologica Sinica, 2004, 19(6): 636-638.
Citation: REN Xue-feng, HU Zhi-hua, TAN Guo-lei, ZHOU Bing, XU Xue-qin, ZHENG Qi-sheng, Zhang Xiao-yong, CHEN De-sheng, CHEN Pu-yan*. Expression of the Domain Gene of Porcine Parvovirus VP2 with the Eukaryotic Vector pIREShyg* .VIROLOGICA SINICA, 2004, 19(6) : 636-638.

猪细小病毒 VP2蛋白主要抗原表位基因真核表达载体的构建及表达*

Expression of the Domain Gene of Porcine Parvovirus VP2 with the Eukaryotic Vector pIREShyg*

  • Using a pair of specific primers designed according to the relevant nucleotide sequences from GenBank, the main antigen domain for VP2 gene of Porcine parvovirus was ampilified with PCR method using the genomic DNA as template. The PCR product was cloned into the expression vector pIREShyg to get a recombinant eukaryotic expression plasmid pIREShyg-VP2, which was then transfected into the CHO-K1 cells. The expressed product was detected by IFA after the positive cell clone was selected with hygromycin. The result revealed that the main antigen domain for VP2 gene of porcine parvovirus was stably expressed in CHO-K1 cells.

  • 加载中
  • 加载中

Article Metrics

Article views(3985) PDF downloads(1180) Cited by(0)

Related
Proportional views
    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Expression of the Domain Gene of Porcine Parvovirus VP2 with the Eukaryotic Vector pIREShyg*

    • 1. Key Laboratory of Animal Disease diagnosis and Immunology, Ministry of Agriculture at Nanjing Agricultural University, Nanjing, Jiangshu 210095, China

    Abstract: Using a pair of specific primers designed according to the relevant nucleotide sequences from GenBank, the main antigen domain for VP2 gene of Porcine parvovirus was ampilified with PCR method using the genomic DNA as template. The PCR product was cloned into the expression vector pIREShyg to get a recombinant eukaryotic expression plasmid pIREShyg-VP2, which was then transfected into the CHO-K1 cells. The expressed product was detected by IFA after the positive cell clone was selected with hygromycin. The result revealed that the main antigen domain for VP2 gene of porcine parvovirus was stably expressed in CHO-K1 cells.

    Relative (20)

    目录

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return