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Immunization and immune activity measurement method

机译:免疫及免疫活性测定方法

摘要

PROBLEM TO BE SOLVED: To immunize a lymphocyte efficiently and to obtain an antigen specific antibody at high concentration by adding an antigen to a culture liquid combining an adjuvant substance and cytokine in order to culture lymphocyte and then measuring immunological activity. ;SOLUTION: When lymphocyte coexists with an antigen in a culture liquid containing a combination of an adjuvant substance and cytokine, lymphocyte can be immunize specifically with high efficiency and a large quantity of antigen speciftc antibody can be obtained. Muramyldipeptide is employed as an adjuvant substance in the lymphocyte. One kind selected from a group of interleukin 2, 4, 6 is employed as the cytokine. Dulbecco MEM medium, Ham F12 medium, or the like, 15 employed as the culture liquid. Keyhole lympet hemocyanin, cholera toxin B subunit, or the like, is employed as the antigen. Lymphocyte in organism or blood (e.g. peripheral blood) is employed as the lymphocyte.;COPYRIGHT: (C)1998,JPO
机译:解决的问题:通过将抗原添加到结合​​佐剂物质和细胞因子的培养液中以培养淋巴细胞,然后测量免疫活性,从而有效地免疫淋巴细胞并以高浓度获得抗原特异性抗体。 ;解决方案:当淋巴细胞和抗原在含有佐剂和细胞因子的培养液中共存时,可以高效地对淋巴细胞进行免疫,从而获得大量抗原特异性抗体。 Muramyldipeptide被用作淋巴细胞中的佐剂。从白介素2、4、6的组中选择一种作为细胞因子。将Dulbecco MEM培养基,Ham F12培养基等用作培养液15。匙孔血蓝蛋白,霍乱毒素B亚基等被用作抗原。生物体或血液(例如外周血)中的淋巴细胞用作淋巴细胞。;版权所有:(C)1998,日本特许厅

著录项

  • 公开/公告号JP3919875B2

    专利类型

  • 公开/公告日2007-05-30

    原文格式PDF

  • 申请/专利权人 森永製菓株式会社;

    申请/专利号JP19970099730

  • 发明设计人 白畑 實隆;橋爪 秀一;

    申请日1997-04-02

  • 分类号G01N33/531;G01N33/53;

  • 国家 JP

  • 入库时间 2022-08-21 21:08:41

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