Fig. 2: Isolation and characterization of EVs from LX-2 cells. | Communications Biology

Fig. 2: Isolation and characterization of EVs from LX-2 cells.

From: Tracking matricellular protein SPARC in extracellular vesicles as a non-destructive method to evaluate lipid-based antifibrotic treatments

Fig. 2

a Size distribution profiles of EVs isolated from differently treated cells (mean ± SD, n = 3). b Quantile subtraction of the yields. c, d SEM (c) and cryo-TEM (d) images of EVs isolated from untreated cells. e–g Protein content and vesicle number in the collected SEC-fractions obtained from untreated (e), quiescent (f), and perpetuated (g) LX-2 (mean ± SD, n = 3). h–j Representative EAF4 fractograms of EV collected from untreated (h), quiescent (i), and perpetuated (j).

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