I plan to assay proliferation dynamics of U-2 OS cells using the IncuCyte platform in a 96 well format. I will be using the IncuCyte NucLight Rapid Red (
https://eu-shop.essenbioscience.com/collections/reagents/products/nuclight-rapid-red-reagent-for-live-cell-nuclear-labeling) for labeling. If you have any experience using this dye for this cell line, what do you think is the optimal seeding density and dye concentration if I plan to record for 5-6 days?