I want to generate a growth curve for fibroblast cell lines isolated from camel ear. Does anyone have a full protocol for how I can do it if I use a 6 well dish?
The above refernce would give you a general protocol. But you need to refine it according to your cell type .(doubling time of your cells, cell numbers that can be plated, etc.)
Please be careful that at the end of the kinetics the cells just reach confluency. otherwise you will have an early plateau. Typically, we seed 25 000 mouse fibroblasts per well and count cells every day (in triplicate) during 4 days (in triplicate). You can use a flow cytometer to do it if it gives you the absolute count of cells.