I am a PhD student and I am mainly working on cell cultures.
Although I have some experience with cell culturing I am currently facing big problems accomplishing a proliferation assay.
To be more exact, I am trying to evaluate the effect of a drug on an adherent cell line by doing crystal violet staining and I am using a 24 well plate for seeding and treating the cells.
I seed the cells at a density of 12.500/cm2 using 1ml of 10% DMEM for each well. I change the medium in order to start the treatment 16-20 hours after seeding the cells.
However what I see then under the microscope is that the cells immediately die after changing the medium and lots of them are swimming in the supernatant having totally lost their attachment from the well ground. That is happening seconds after changing the medium and applies not only for the cells treated with the drug but also for my control cells treated with DMSO (0,01% final concentration).
The strange thing is that I haven't so far noticed something like that (or at least to that extent) when working with 96-well plates.
Could it be that I do not leave the cells attach enough in the wells? Or that I am pipetting the medium too violently causing most of the cells to detach?
Does anyone more experienced than me have any idea or has already faced a similar problem?
I would really appreciate any kind of help.













