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Helper-free Production of Laboratory Grade AAV and Purification by Iodixanol Density Gradient Centrifugation.
Crosson, Sean M; Dib, Peter; Smith, J Kennon; Zolotukhin, Sergei.
Afiliación
  • Crosson SM; Department of Pediatrics, Division of Cell and Molecular Therapy, University of Florida, Gainesille, FL, USA.
  • Dib P; Department of Anatomy and Cell Biology, University of Florida, Gainesille, FL, USA.
  • Smith JK; Department of Biochemistry and Molecular Biology, University of Florida, Gainesille, FL, USA.
  • Zolotukhin S; Department of Pediatrics, Division of Cell and Molecular Therapy, University of Florida, Gainesille, FL, USA.
Mol Ther Methods Clin Dev ; 10: 1-7, 2018 Sep 21.
Article en En | MEDLINE | ID: mdl-30073177
ABSTRACT
Adeno-associated virus (AAV) is one of the most promising gene therapy vectors and is widely used as a gene delivery vehicle for basic research. As AAV continues to become the vector of choice, it is increasingly important for new researchers to have access to a simplified production and purification protocol for laboratory grade recombinant AAV. Here we report a detailed protocol for serotype independent production of AAV using a helper-free HEK293 cell system followed by iodixanol gradient purification, a method described earlier.1 While the core principals of this mammalian AAV production system are unchanged, there have been significant advancements in the production and purification procedure that serve to boost yield, maximize efficiency, and increase the purity of AAV preps. Using this protocol, we are able to constantly obtain high quantities of laboratory grade AAV particles (>5 × 1012 vg) in a week's time, largely independent of serotype.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Mol Ther Methods Clin Dev Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Mol Ther Methods Clin Dev Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos