Does anyone know if there has to be a specified seeding density for the senescence-associated beta galactosidase assay performed in a 96-well plate? Or does any seeding density generally work for the assay? Thanks!
if there is no information given there, I would go for whatever is "healthy" for your cell line; for most cell lines this would be something between 60 and 80% confluence - you will most definitely find detailed info on that for your specific cell line online!