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Yonsei Medical Journal ; : 790-794, 2016.
Artículo en Inglés | WPRIM | ID: wpr-205734

RESUMEN

Recombinant gene expression using adeno-associated viruses (AAVs) has become a valuable tool in animal studies, as they mediate safe expression of transduced genes for several months. The liver is a major organ of metabolism, and liver-specific expression of a gene can be an invaluable tool for metabolic studies. AAV-DJ is a recombinant AAV generated by the gene shuffling of various AAV serotypes and shares characteristics of AAV2 and AAV8. AAV-DJ contains a heparin-binding domain in its capsid, which suggests that a heparin column could be used for the purification of the AAV. Given that AAV-DJ has been only recently available, relatively little is known about the optimal preparation/purification and application of AAV-DJ. Here, we present a simple large-scale preparation method that can generate 3×10(13) viral particles for in vivo experiments and demonstrate liver-specific gene expression via systemic injection in mice.


Asunto(s)
Animales , Humanos , Ratones , Cápside , Proteínas de la Cápside/genética , Dependovirus/genética , Expresión Génica , Vectores Genéticos , Genoma Viral/genética , Células Hep G2 , Hígado/metabolismo , Ratones Endogámicos C57BL
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