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The culture solution for the neurocyte, the production manner and culture manner null of the neurocyte which uses

机译:神经细胞的培养液,所用神经细胞的生产方式和培养方式无效

摘要

PROBLEM TO BE SOLVED: To obtain the subject culture liquid capable of stably performing the culture of central nerve cells by blending albumin to a supernatant of a culture collected by culturing primary astroglia cells in a nutrition medium added with insulin and transferrin. ;SOLUTION: This culture liquid for nerve cells capable of stably performing a culture of central nerve cells, excellent in extending property of neuraxon, capable of rapidly forming synapses in a low density culture, and obtaining the cells forming a neural network in a high density culture, is obtained by adding insulin and transferrin to one or more kinds of nutrition media such as Eagle basal medium(MEM), Dulbecco modified Eagle medium(DMEM) and Ham F-12 medium, culturing primary astroglia cells, then collecting the supernatant of the medium, blending albumin to the supernatant of the medium and further adding progesterone, insulin, transferrin, selenious acid (salt), a superoxide dismutase and a catalase thereto.;COPYRIGHT: (C)1997,JPO
机译:解决的问题:通过将白蛋白掺入通过在添加有胰岛素和转铁蛋白的营养培养基中培养原代星形胶质细胞而收集的培养物的上清液,从而获得能够稳定地进行中枢神经细胞培养的主题培养液。 ;解决方案:这种神经细胞培养液能够稳定地进行中枢神经细胞的培养,神经氨酸的延伸特性极佳,能够在低密度培养物中快速形成突触,并获得高密度形成神经网络的细胞通过将胰岛素和转铁蛋白添加到一种或多种营养培养基(例如Eagle基础培养基(MEM),Dulbecco改良的Eagle培养基(DMEM)和Ham F-12培养基)中,培养原代星形胶质细胞,然后收集培养基,将白蛋白掺入培养基的上清液中,并进一步向其中添加孕酮,胰岛素,转铁蛋白,亚硒酸(盐),超氧化物歧化酶和过氧化氢酶。;版权:(C)1997,JPO

著录项

  • 公开/公告号JP3093974B2

    专利类型

  • 公开/公告日2000-10-03

    原文格式PDF

  • 申请/专利权人 住友ベークライト株式会社;

    申请/专利号JP19960147158

  • 发明设计人 渡辺 芳明;

    申请日1996-06-10

  • 分类号C12N5/06;

  • 国家 JP

  • 入库时间 2022-08-22 02:06:21

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