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腺相关病毒的生产、纯化及滴度测定。

Adeno-Associated Virus Production, Purification, and Titering.

作者信息

Chen Yong Hong, Keiser Megan S, Davidson Beverly L

机构信息

The Raymond G. Perelman Center for Cellular and Molecular Therapeutics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Curr Protoc Mouse Biol. 2018 Dec;8(4):e56. doi: 10.1002/cpmo.56. Epub 2018 Nov 29.

Abstract

Adeno-associated virus (AAV) vectors are exemplary tools for studying gene function in vivo and are particularly favorable for transferring genes of interest into brain tissues. They have shown great promise as a gene therapy vector for preclinical and clinical applications. However, the ability to use this tool is often hampered because the viruses themselves are not readily available. Many methods have been developed for AAV production. Here, we describe a simple method for small- to medium-scale (10 -10 viral particles) production of AAV based on Polyethylenimine Max (PEI Max)-mediated triple transfection of HEK 293 cells and purification with iodixanol gradient ultracentrifugation. These methods will provide users with ample material of sufficient quality for performing in vivo gene transfer. © 2018 by John Wiley & Sons, Inc.

摘要

腺相关病毒(AAV)载体是研究体内基因功能的典型工具,特别有利于将感兴趣的基因导入脑组织。它们作为基因治疗载体在临床前和临床应用中显示出巨大的潜力。然而,使用这一工具的能力常常受到阻碍,因为病毒本身不易获得。已经开发出许多生产AAV的方法。在此,我们描述一种基于聚乙烯亚胺Max(PEI Max)介导的HEK 293细胞三重转染并用碘克沙醇梯度超速离心法纯化,用于中小规模(10⁶ - 10⁸病毒颗粒)生产AAV的简单方法。这些方法将为用户提供足够数量和质量的材料用于进行体内基因转移。© 2018约翰威立父子出版公司

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