ive tried many protocols but yet they are not efficient.i want to seed the cells in 96-plate but i cant obtain enough cells even though the flask seems 90% confluent.
We normally use trypsin/EDTA solution to efficiently detach VERO cells. The volume used depends on your culture flasks. We drain the flask media and rinse it with sterile PBS, then we add the appropriate volume of trypsin and incubate the flask at 35ºC at 5% CO2 for up to 3 min, for cells detachment. The trypsin is neutralized when the new media is added to the flask, with fetal bovine serum.