Poly-L-lysine is know for the seeding of cells but I just read an article relating the fact that cells could degrade Poly-L-lysine on coverslips during the culture day to get the cells to confluence. I saw that poly-D-lysine could be an alternative. Does someone already have experience with these two kinds of coating and can tell me which one is the best?

The purpose is to make staining of cells for microscopy imaging.

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