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Regulated expression of proteins in mammalian cells stably transfected.

机译:稳定转染的哺乳动物细胞中蛋白质的调节表达。

摘要

THE invention is in the field of genetic recombinants MATERIALS, ESPECIALLY FOR USE IN GENE THERAPY. VECTORS FOR TRANSFER USED IN ADDITION TO CELL GENETIC INFORMATION IN THE FIELD OF GENE THERAPY A VIRUS often rely on. A GROUP OF VIRUS HAS BEEN PROPOSED FOR USE FOR Transfection is the group of parvovirus, and in particular has proposed the use of adeno associated virus. The invention describes PROCEDURES AND ARRANGEMENTS FOR IMPROVED GENE THERAPY AND PREPARE FOR PRODUCTS FOR USE IN gene therapy BASED MATERIALS USING parvovirus. The invention describes a particular way regulated expression of genes under the control of the combination of a repressor and an activator RADICAL RADICAL IN PARTICULAR FOR EXPRESSION OF PRODUCTS ARE FOR TOXIC host cell WHICH ARE EXPRESSED IN. This makes it possible to achieve a stable transfection for protein expression TOXIC parvovirus, SO TO, DESCRIBED a cell line Encapsulation TO PRODUCE recombinant Parvovirus, INCLUDING adeno partners and VIRUSES RESULTING IN ITS INTERIOR.
机译:本发明属于基因重组材料领域,特别是用于基因治疗的材料。病毒载体通常依赖于在基因治疗领域中用于细胞遗传信息的转移载体。已提议将一组病毒用于细小病毒转染,尤其是已提出使用腺伴随病毒。本发明描述了改进的基因治疗的方法和装置,以及制备了用于使用细小病毒的基因治疗为基础的材料的产品的制备方法。本发明描述了在阻遏物和活化剂的组合的控制下调节基因表达的特定方式。自由基特别是对于表达产物的表达是针对有毒宿主细胞表达的。这使得有可能实现蛋白质表达有毒性的细小病毒的稳定转染,从而描述了一种细胞系包膜,以生产重组细小病毒,包括腺配偶体和导致其内部的病毒。

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