首页> 外国专利> GENE-THERAPEUTIC DNA-VECTOR BASED ON GENE-THERAPEUTIC DNA-VECTOR VTVAF17, CARRYING TARGET GENE CAS9 FOR HETEROLOGOUS EXPRESSION OF THIS TARGET GENE IN HUMAN AND ANIMAL CELLS IN IMPLEMENTING VARIOUS METHODS OF GENOMIC EDITING, METHOD OF PRODUCING AND USING GENE-THERAPEUTIC DNA VECTOR, ESCHERICHIA COLI SCS110-AF/VTVAF17-CAS9 STRAIN, CARRYING GENE-THERAPEUTIC DNA VECTOR, METHOD FOR PREPARING THEREOF, METHOD FOR PRODUCTION ON INDUSTRIAL SCALE OF GENE-THERAPEUTIC DNA VECTOR

GENE-THERAPEUTIC DNA-VECTOR BASED ON GENE-THERAPEUTIC DNA-VECTOR VTVAF17, CARRYING TARGET GENE CAS9 FOR HETEROLOGOUS EXPRESSION OF THIS TARGET GENE IN HUMAN AND ANIMAL CELLS IN IMPLEMENTING VARIOUS METHODS OF GENOMIC EDITING, METHOD OF PRODUCING AND USING GENE-THERAPEUTIC DNA VECTOR, ESCHERICHIA COLI SCS110-AF/VTVAF17-CAS9 STRAIN, CARRYING GENE-THERAPEUTIC DNA VECTOR, METHOD FOR PREPARING THEREOF, METHOD FOR PRODUCTION ON INDUSTRIAL SCALE OF GENE-THERAPEUTIC DNA VECTOR

机译:基于基因-治疗性DNA-载体VTVAF17的基因治疗性DNA-载体,携带目标基因CAS9在人和动物细胞中异源表达该靶基因,以实现各种基因编辑方法,制备方法和制备方法,大肠杆菌(Escherichia)COLI SCS110-AF / VTVAF17-CAS9菌株,携带基因-治疗性DNA矢量的载体,其制备方法,基因-治疗性DNA矢量的工业规模生产方法

摘要

FIELD: biotechnology; medicine; agriculture.;SUBSTANCE: invention refers to genetic engineering and can be used in biotechnology, medicine and agriculture to develop gene therapy preparations. Presented is a gene-therapeutic DNA vector based on the gene-therapeutic DNA vector VTvaf17, carrying the target Cas9 gene for heterologous expression of this target gene in human and animal cells when implementing various methods of genomic editing. Gene-therapeutic DNA vector VTvaf17-Cas9 has the nucleotide sequence SEQ ID No. 1. Invention also discloses a method of producing said vector, use of a vector, an Escherichia coli strain carrying said vector, as well as a method of producing said vector on an industrial scale.;EFFECT: invention can be used for safe application for human and animal genetic therapy.;8 cl, 12 dwg, 14 ex
机译:领域:生物技术;药物;物质:发明是指基因工程,可以用于生物技术,医学和农业中以开发基因疗法的制剂。提出了一种基于基因治疗性DNA载体VTvaf17的基因治疗性DNA载体,当实施各种基因组编辑方法时,该载体携带目标Cas9基因以在人和动物细胞中异源表达该目标基因。基因治疗DNA载体VTvaf17-Cas9具有核苷酸序列SEQ ID No.1。本发明还公开了生产所述载体的方法,载体的使用,携带所述载体的大肠杆菌菌株以及生产所述载体的方法。效果:本发明可用于人类和动物基因治疗的安全应用。; 8 cl,12 dwg,14 ex

著录项

  • 公开/公告号RU2730663C2

    专利类型

  • 公开/公告日2020-08-24

    原文格式PDF

  • 申请/专利权人 CELL AND GENE THERAPY LTD;

    申请/专利号RU20180147083

  • 发明设计人 SAVELIEVA NATALIA (AT);

    申请日2018-12-27

  • 分类号C12N15/12;C12N15/70;C12N1/21;A61K48;C12R1/19;

  • 国家 RU

  • 入库时间 2022-08-21 11:02:20

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