I am trying to make an exosome that expresses my gene of interest. I transfect the hek293 with a plasmid that has my gene of interest. After transfection, I isolate the exosomes from the cell culture supernatant by PEG 4000 isolation method. But exosome pellet is not visible after isolation. Anyone here has faced the same issue. How to solve that issue. Need help in this regard.

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