Hi all,
It was my first time to passage H9 cultured on iMatrix-511(laminin 511) coated wells/dish under feeder-free system, and I found that most colonies were not detached from the well after ReleSR digestion even for a prolonged digestion time (almost 10 min in 37 C, incubator).
So, what is best way to passage H9 cells on iMatrix-511 coated wells? I prefer to digest colonies into cell-clumps, Not into single cells.
Thanks!!!