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Chinese Journal of Biotechnology ; (12): 982-986, 2009.
Artigo em Chinês | WPRIM | ID: wpr-286613

RESUMO

After sequencing, we amplified and cloned foot-and-mouth disease virus (FMDV) O/QYYS/s/06 whole genome by three fragments. These three fragments were cloned into vector P43 one by one to construct recombinant plasmid P43C, which carried the full-length cDNA of FMDV O/QYYS/s/06. Then, plasmid P43C and plasmid T7 expressing T7 RNA polymerase were co-transfected into BHK-21 cells. After 48 h, we harvested the culture broth from transfected BHK-21 cells and inoculated into 2-3 day-old sucking mice. After four generation passage, the virus harvested from sucking mice was confirmed to be type O FMDV by the indirect hemagglutination test, sucking mice's neutralization test and sequencing. The results showed that we have successfully constructed the full-length cDNA clone of FMDV O/QYYS/s/06 strain.


Assuntos
Animais , Camundongos , Animais Recém-Nascidos , Clonagem Molecular , DNA Complementar , Genética , DNA Viral , Genética , Febre Aftosa , Virologia , Vírus da Febre Aftosa , Classificação , Genética , Virulência , Transcrição Gênica , Transfecção
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