I thawed microvascular endothelial cells from the -80 freezer and spun the suspension in DMEM down at 150G for 5 minutes. After this I added 2 mL EGM-2MV medium to the cells and resuspended it. Then I put the suspension in a Burker counting chamber and I saw all these floating pieces. I checked the medium and the glass, but that wasn't it, so it has to be the cells.

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