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MEGAKARYOCYTE DIFFERENTIATION AND PROLIFERATION FACTOR AND ITS PRODUCTION

机译:巨核细胞的分化增殖因子及其产生

摘要

PURPOSE: To provide the subject new proliferation factor obtained from a culture liquid prepared by culturing mouse spleen cell in the presence of a mitogen, effective in selectively differentiating and proliferating megakaryocyte, free from proliferation activity to other cells such as leukocyte and useful for the treatment of thrombocytopenia, etc. ;CONSTITUTION: A mouse-originated spleen cell is cultured in a medium such as RPM11640 medium in the presence of pokeweed-mitogen, the culture liquid is centrifuged, the supernatant is collected and incorporated with ammonium sulfate and the formed precipitate is collected. The precipitate is dissolved in 0.14M Nacl solution containing 10mM phosphate buffer solution and dialyzed with the solution to remove the ammonium sulfate. The dialyzed liquid is adsorbed to a DEAE sepharose column, an adsorbed fraction eluted with 0.5M Nacl aqueous solution containing 10mM phosphate buffer solution is collected and a protein component is separated from the fraction to obtain the objective megakaryocyte differentiation and proliferation factor inactivated by protease treatment and enabling selective differentiation and proliferation of megakaryocyte.;COPYRIGHT: (C)1994,JPO&Japio
机译:目的:提供从通过在有丝分裂原的存在下培养小鼠脾细胞而制备的培养液中获得的本发明的新的增殖因子,其有效地选择性分化和增殖巨核细胞,对白细胞等其他细胞没有增殖活性,可用于治疗组成:小鼠起源的脾细胞在商陆有丝分裂原存在下于RPM11640培养基中培养,离心培养液,收集上清液并与硫酸铵合并,形成沉淀被收集。将沉淀物溶解在含有10mM磷酸盐缓冲溶液的0.14M Nacl溶液中,并用该溶液渗析以除去硫酸铵。将透析液吸附到DEAE琼脂糖柱上,收集用0.5M Nacl水溶液洗脱的吸附级分,所述Nacl水溶液含有10mM磷酸盐缓冲溶液,并从级分中分离蛋白质组分,从而通过蛋白酶处理使目标巨核细胞分化和增殖因子失活。并能使巨核细胞选择性分化和增殖。;版权所有:(C)1994,日本特许厅&日本apio

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