I want to use an IP3R inhibitor (xerospongin C) in an in vitro calcium release assay with CHO-K1 cells. I accidentally dissolved the small amount we received in DMSO at a concentration which means the cells will be exposed to 2% DMSO when added at the standard concentration this compound is used. It might be OK but I'd prefer to avoid it.
We use a freeze dryer in the lab to lyophilise peptides in water. Can I use this to remove the DMSO, then resuspend to make a more concentrated stock to use in my experiment?
The volume needing to be removed is ~200uL.
I've seen a few comments suggesting variously that DMSO can & can't be removed by lyophilisation. If anyone can tell me if in my circumstances it should be possible, I'd be very grateful (and if I need to do anything extra, e.g. add a bit of water first).
Thanks!