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IN VITRO CULTURE METHOD FOR MYCOBACTERIUM LEPRAE

机译:支原体肺炎球菌的体外培养方法

摘要

The object is to establish a method for establishing a cell line having low proliferation ability and low-temperature resistance, and to provide a simple and long-term in vitro culture method for Mycobacterium leprae. Disclosed is a method for establishing a low-temperature-resistant, (very-)low-proliferative cell line, which is characterized by culturing a tumor cell produced from a human hemangiosarcoma subcutaneously transplantable into an SCID (severe combined immunodeficiency disease) mouse in a culture medium containing a mouse hemangiosarcoma cell line ISOS-1 culture supernatant, selecting a cell that is not detached by the trypsin-EDTA treatment from cultured cells, and subculturing the cell line while reducing the amount of the ISOS-1 culture supernatant to be added to the culture medium. Also disclosed is a cell line produced by the method. Further disclosed is a culture method for Mycobacterium leprae.
机译:目的是建立用于建立具有低增殖能力和低温耐受性的细胞系的方法,并且提供一种用于麻风分枝杆菌的简单且长期的体外培养方法。本发明公开了一种建立耐低温(非常)低增殖细胞系的方法,其特征在于,将由人血管肉瘤产生的肿瘤细胞皮下移植入SCID(严重的合并免疫缺陷病)小鼠体内。含有小鼠血管肉瘤细胞系ISOS-1培养上清液的培养基,从培养的细胞中选择未通过胰蛋白酶-EDTA处理分离的细胞,并在减少添加的ISOS-1培养上清液量的同时对细胞系进行传代培养到培养基。还公开了通过该方法产生的细胞系。还公开了麻风分枝杆菌的培养方法。

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