Method for producing viral vector
    5.
    发明授权
    Method for producing viral vector 有权
    生产病毒载体的方法

    公开(公告)号:US09399780B2

    公开(公告)日:2016-07-26

    申请号:US14381721

    申请日:2013-03-14

    申请人: TAKARA BIO INC.

    摘要: The present invention provides a method for producing a virus vector, which involves a step of culturing a cell capable of producing the virus vector in a culture medium containing a retinoic acid compound, a histone deacetylase-inhibiting substance and a substance capable of forming a chelate; and a culture medium for use in the production of a virus vector, which is characterized by containing a retinoic acid compound, a histone deacetylase-inhibiting substance and a substance capable of forming a chelate as active ingredients.

    摘要翻译: 本发明提供一种病毒载体的制备方法,其包括在含有维甲酸化合物,组蛋白脱乙酰酶抑制物质和能够形成螯合物的培养基中培养能够产生病毒载体的细胞的步骤 ; 以及用于生产病毒载体的培养基,其特征在于含有视黄酸化合物,组蛋白脱乙酰酶抑制物质和能够形成螯合物的物质作为活性成分。

    Method for gene transfer
    7.
    发明授权
    Method for gene transfer 有权
    基因转移方法

    公开(公告)号:US09228206B2

    公开(公告)日:2016-01-05

    申请号:US14457453

    申请日:2014-08-12

    申请人: TAKARA BIO INC.

    CPC分类号: C12N15/86 C12N2740/10043

    摘要: Disclosed is a simple and highly efficient method for introducing a gene into a target cell using a retrovirus vector. The method comprises the steps of (a) placing a liquor containing a retrovirus vector having a foreign gene carried thereon into a bag for cell culture on which a retrovirus-binding substance has been immobilized, and incubating the liquor at a temperature lower than 25° C. for 8-48 hours, thereby producing a culture bag having the retrovirus vector bound thereto, (b) adding a target cell to the culture bag that has been produced in step (a) and incubating the culture bag for 8 hours or less, and (c) flipping the culture bag upside down and incubating the culture bag. The gene introduction method is useful particularly in medicine, cell technology, gene technology, and embryologic technology.

    摘要翻译: 公开了使用逆转录病毒载体将基因导入靶细胞的简单且高效的方法。 该方法包括以下步骤:(a)将含有携带有外来基因的逆转录病毒载体的液体放入已经固定有逆转录病毒结合物质的细胞培养袋中,并在低于25℃的温度下培养该液体 制备具有结合反转录病毒载体的培养袋,(b)向步骤(a)中生产的培养袋中加入靶细胞,并将培养袋孵育8小时以下 ,(c)颠倒培养袋并培养培养袋。 基因导入方法特别适用于医学,细胞技术,基因技术和胚胎学技术。