I got competent cells of E. Coli induced with IPTG to express B-amyloid peptide and I stained them with ThS and propidium iodide after permeabilizated with Triton x 100; however, when I want to observe them trought the microscope, they appear like aggregates and it's not possible to see clearly inclusion bodies nor the cell structure. Can you suggest some method or reactant which I could add to this solution for improve the visualization?

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