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Nutrient medium null for central neurocyte

机译:营养液中枢神经细胞无效

摘要

PURPOSE: To obtain the subject new medium capable of achieving continuously stable adhesion of nerve cell, extension of projection of nerve and survival maintenance without requiring coating of cell adherent protein, comprising a cultured supernatant liquid of established hepatocyte prepared by serum-free culture as an active ingredient. ;CONSTITUTION: The objective medium comprising a cultured supernatant liquid of established prepared by serum-free culture as an active ingredient. To be concrete, a hepatocyte such as NTCC clone 1,469 is cultured in 10% bovine fatal serum-containing DME/F-12 medium until the hepatocyte becomes semiconfluent, the medium is changed into a serum-free medium from which serum is removed, the hepatocyte is cultured for 2-3 days and the cultured supernatant liquid is used as an active ingredient for a medium for central neurocyte.;COPYRIGHT: (C)1993,JPO&Japio
机译:用途:为了获得能够实现神经细胞连续稳定粘附,神经投射扩展和维持生存而无需涂覆细胞粘附蛋白的主题新培养基,该培养基包含通过无血清培养制备的成熟肝细胞培养上清液。有效成分。 ;组成:目标培养基,其包含通过无血清培养制备的经培养的上清液作为活性成分。具体而言,将肝细胞(例如NTCC克隆1,469)在含10%牛致命性血清的DME / F-12培养基中培养,直到肝细胞半融合为止,然后将其换成无血清培养基,从中除去血清,肝细胞培养2-3天,培养的上清液用作中枢神经细胞培养基的活性成分。版权所有:(C)1993,日本特许厅,日本

著录项

  • 公开/公告号JP2649880B2

    专利类型

  • 公开/公告日1997-09-03

    原文格式PDF

  • 申请/专利权人 BAIO MATERIARU KENKYUSHO KK;

    申请/专利号JP19910301247

  • 发明设计人 WATANABE YOSHIAKI;

    申请日1991-10-22

  • 分类号C12N5/06;

  • 国家 JP

  • 入库时间 2022-08-22 03:29:27

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