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H1N1亚型猪流感病毒血凝素基因的克隆与表达
引用本文:马祥,顾万军,刘镇明,黄良宗,彭启明.H1N1亚型猪流感病毒血凝素基因的克隆与表达[J].动物医学进展,2006,27(8):73-76.
作者姓名:马祥  顾万军  刘镇明  黄良宗  彭启明
作者单位:1. 华南农业大学兽医学院,广东广州,510642;佛山科学技术学院,广东佛山,528231
2. 佛山科学技术学院,广东佛山,528231
3. 华南农业大学兽医学院,广东广州,510642
摘    要:应用RT-PCR方法扩增了1株H1N1亚型猪流感病毒的血凝素基因,并克隆到pMD 18-T Simple载体中,经PCR、酶切和测序验证克隆正确后,亚克隆到真核表达载体pcDNA3.1( )中,构建了重组质粒pcDNA-HA。在脂质体作用下重组质粒pcDNA-HA转染Vero细胞。间接免疫荧光试验结果表明,血凝素基因在Vero细胞中成功进行了瞬时表达,这为猪流感病毒DNA疫苗的进一步研究奠定了基础。

关 键 词:猪流感病毒  血凝素基因  克隆  表达  Vero细胞
文章编号:1007-5038(2006)08-0073-04
收稿时间:2006-03-16
修稿时间:2006年3月16日

Cloning and Expressiong of Subtype H1N1 SIV HA Gene in Vero Cells
MA Xiang,GU Wang-jun,LIU Zhen-ming,HUANG Liang-zong,PENG Qi-ming.Cloning and Expressiong of Subtype H1N1 SIV HA Gene in Vero Cells[J].Progress In Veterinary Medicine,2006,27(8):73-76.
Authors:MA Xiang  GU Wang-jun  LIU Zhen-ming  HUANG Liang-zong  PENG Qi-ming
Institution:1. College of Veterinary Medicine,South China Agriculture University , Guangzhou,Guang dong , 510642 , China 2. Foshan College of ,Science and Technology,Foshan,Guangdong,528231,China
Abstract:The HA gene of subtype H1N1 SIV was amplified by RT-PCR assay and sequently subcloned into vector pcDNA3.1( ) to construct expression plasmid pcDNA-HA.Mediated with Lipofectamine TM 2000,pcDNA-HA was introduced into Vero cells.And the indirect immuno fluorescent assay analysis showed that HA gene was been expressed transiently in Vero cells.
Keywords:SIV  HA gene  clone  expression  Vero cells
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