Hi Toot!
First of all, congratulation on the ComBO publication, truly impressive validation!
I have two questions regarding the cells released from the organoids.
1. I was wondering if you routinely observe great amount of released cells in the media, even without the usage of the 3D-printed fluidic device. We observe it already at DIV21 in a line-dependent way (some lines released a lot of cells, others none) and they are highly enriched in hematopoietic cells, but we do not use any fluidic device or shaking, so I was wondering your experience with this.
2. I was wondering if you could share the protocol you used for the Cytospin (speed and centrifugation time), because in my experience with Cytospin cells smash and loose their morphology once on the slide.
Thank you in advance!
Cecilia