When you harvest splenocytes from a mouse or so, why is it important when teasing out the cells (via glass slides with frosted edges) not to get cavitation/aerosols? It is going to be centrifuged (isn't that the point of the "wash(s)"?) anyway, so what's the big emphasis of it about?
Cheers,
Phil


Mike Taylor
Dave Warburton
David Wynick



