首页> 外国专利> DNA or fragments thereof, encoding the human erythropoietin, vectors, host cells or cell lines, DNAc or fragments thereof, encoding the human erythropoietin, human recombined erythropoietin, processes for obtaining human erythropoietin and human recombined erythropoietin, pharmaceutical composition and process for obtaining thereof

DNA or fragments thereof, encoding the human erythropoietin, vectors, host cells or cell lines, DNAc or fragments thereof, encoding the human erythropoietin, human recombined erythropoietin, processes for obtaining human erythropoietin and human recombined erythropoietin, pharmaceutical composition and process for obtaining thereof

机译:编码人促红细胞生成素的DNA或其片段,载体,宿主细胞或细胞系,编码人促红细胞生成素的DNAc或其片段,人重组促红细胞生成素,获得人促红细胞生成素和人重组促红细胞生成素的方法,药物组合物及其获得方法

摘要

The present invention relates to biotechnology, medical and biological industry, medicine and, particularly to cloned DNA, encoding human erythropoietin, expressions of the indicated DNA and in vitro obtaining of active human erythropoietin. of DNA genome fragments from human fetal liver and DNAc fragments, providing exceptionally high levels of the erythropoietin expression into the mammal cells, it is obtained the cell line of the Chinese hamster ovary CHO, producing recombined EPO (CHO EPO Cla 4a4.02-7). As a result of the DNA cloned fragments expression into the mammal cells there was obtained the O-glycosylated EPO, having a specific activity of at least 200000 units/mg and the pharmaceutical composition, wherein the above-mentioned recombined EPO is used as active ingredient.The result of the invention consists in levels growth of the active human erythropoietin expression in vitro as well as in removal of adverse reaction during treatment with human recombined erythropoietin.
机译:本发明涉及生物技术,医学和生物工业,医学,特别是涉及编码人促红细胞生成素的克隆DNA,所示DNA的表达以及在体外获得活性人促红细胞生成素。人胎儿肝脏的DNA基因组片段和DNAc片段的表达,在哺乳动物细胞中提供了异常高水平的促红细胞生成素表达,它获得了中国仓鼠卵巢CHO细胞系,产生了重组EPO(CHO EPO Cla 4a4.02-7 )。通过DNA克隆片段在哺乳动物细胞中的表达,获得了具有至少200000单位/ mg的比活性的O-糖基化的EPO和药物组合物,其中上述重组的EPO被用作活性成分。本发明的结果在于体外活性人促红细胞生成素表达的水平增长以及在用人重组促红细胞生成素治疗期间消除不良反应。

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