ive been having issues with seeding HeLa cells in 24well and 6well plates.
For example:
- i use trypsin/versene to trypsinize my cells
- take 100ul of the cells and dilute it 1:10
- count my cells with hemacytometer
- then i calculate the cells required for seeding and i always make sure to add a little bit more to make in case of pipetting error/cell death (our lab doesnt use trypan blue)
then i seed my cells at 50% confluency then the next day my cells are not even 90-100% confluent
they are are pretty much 20-50% confluent; i dont know wats going on. wat am i doing wrong????
i tried mixing the cells before i seed
i tried using less trypsin
but they havent worked
the only way my seeding works is to supersaturate the wells with cells and aspirate cells that havent adhered













