AAV Vectors For In Vitro and In Vivo Uses
Failed to add items
Sorry, we are unable to add the item because your shopping cart is already at capacity.
Add to basket failed.
Please try again later
Add to wishlist failed.
Please try again later
Remove from wishlist failed.
Please try again later
Adding to library failed
Please try again
Follow podcast failed
Unfollow podcast failed
-
Narrated by:
-
By:
When combined with modern technology for gene expression including cells-specific promoters as well as the Cre/lox system and genome-editing, AAVs provide a feasible quick, cost-effective, and affordable alternative to conditional knockouts or the transgenic mice models. But, there are many obstacles to widespread AAV cell line use, including ineffective methods for purification and small viral numbers. We present an improved procedure to make AAVs with serotypes that are not dependent on their genotypes.
adbl_web_anon_alc_button_suppression_t1
No reviews yet