I want to use secreted bioluminescence to identify successfully transfected cells, however that would require each individual cell is in its own little isolated well so that the successfully transfected cells don't pump luciferase into the same medium that the unsuccessfully transfected cells reside in. Assuming I have the fortitude to manually separate my cells, does anybody know what I should separate them into? Like a 96 well plate, but instead of 96 wells it has like 1000 tiny wells?

Thanks.