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公开(公告)号:US20100159467A1
公开(公告)日:2010-06-24
申请号:US12633890
申请日:2009-12-09
IPC分类号: C12Q1/68
CPC分类号: C07K14/005 , C12N7/00 , C12N2510/02 , C12N2770/24221 , C12N2770/24222 , C12P21/02 , G01N33/5767
摘要: A process for screening anti-HCV agents, including the steps of introducing a compound to be tested for its anti-HCV properties with transformed Vero/6418 cells, having a nucleic acid selected from the group consisting of a nucleic acid coding for the structural and non-structural proteins of the HCV, a nucleic acid coding for the non-structural proteins of the HCV, and a replicon containing a resistance gene to an antibiotic and a nucleotide sequence coding for the non-structural proteins of the HCV; extracting total RNA of the cells; and analyzing any reduction of the rate, of synthesis of the RNA of the HCV of the cells relative to a control value corresponding to the rates of synthesis of the RNAs of the HCV of the cells in the absence of the tested compound.
摘要翻译: 一种用于筛选抗HCV药物的方法,包括以下步骤:用转化的Vero / 6418细胞引入待测化合物的抗-HCV特性的化合物,所述方法具有选自编码结构的核酸和 HCV的非结构蛋白,编码HCV的非结构蛋白的核酸和含有抗生素抗性基因的复制子和编码HCV的非结构蛋白的核苷酸序列; 提取细胞的总RNA; 并且相对于在不存在测试化合物的情况下相对于细胞的HCV合成速率的对照值,分析细胞的HCV合成速率的任何降低。