Hi everyone.

I am having trouble with my exosomes since they have a high tendency to aggregate, as observed in DLS data and FESEM images (size ranges from 200 nm to 2 micrometer). I have tried mild sonication or vortexing but the problem seems to persist.

For further clarification, exosomes have been derived from UC-MSCs and isolated with ultracentrifuging.

I would be thankful If anyone could share probable solutions.

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