Hi Everyone,

I am planning to make organotypic slices from brain organoids derived from iPSCs to grow them on multi-array electrode plates. I always see in protocols the slicing of tissue in cold aCSF rather than in culture media. Can anyone explain the pros and cons? Has anyone tried using Rock inhibitor to increase the viability of the tissues? I would appreciate any help and recommendations :).

All the best,

Tania Rizo

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