CPC C12N 7/00 (2013.01) [C12N 1/06 (2013.01); C12N 15/86 (2013.01); C12N 2750/14041 (2013.01); C12N 2750/14152 (2013.01)] |
AS A RESULT OF REEXAMINATION, IT HAS BEEN DETERMINED THAT: |
Claim 4 is cancelled. |
Claims 1 and 18 are determined to be patentable as amended. |
Claims 2, 3, 5-17 and 19-21, dependent on an amended claim, are determined to be patentable. |
1. A method for adeno-associated virus (AAV) vector production, the method comprising:
(a) culturing mammalian cells in suspension culture;
(b) transfecting the mammalian cells with an AAV transfer vector using a transfection reagent [ , wherein the transfection reagent comprises a cationic lipid] ;
(c) contacting transfected cells with an enhancer;
(d) culturing the transfected cells in suspension culture for a period of time sufficient for expression of the AAV vector, thereby producing a transfected AAV cell culture; [ and]
(e) harvesting AAV from the transfected AAV cell culture;
wherein the enhancer comprises one or more of a histone deacetylase (HDAC) inhibitor, sodium propionate, and caffeine.
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18. A method for adeno-associated virus (AAV) vector production, the method comprising:
(a) culturing mammalian cells in suspension culture;
(b) transfecting the mammalian cells with an AAV transfer vector using a transfection reagent [ , wherein the transfection reagent comprises a cationic lipid] ;
(c) contacting transfected cells with an enhancer;
(d) culturing the transfected cells in suspension culture for a period of time sufficient for expression of the AAV vector, thereby producing a transfected AAV cell culture; [ and]
(e) harvesting AAV from the transfected AAV cell culture, wherein the cells are not centrifuged prior to harvesting AAV.
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