Skip to main content
. 2020 Mar 2;10(3):88. doi: 10.3390/metabo10030088

Figure 1.

Figure 1

Cell and extracellular vesicles (EV) pellets were re-suspended in a Radioimmunoprecipitation assay (RIPA) buffer and subjected to SDS-PAGE and Western blot analysis. Samples were transferred to nitrocellulose membranes and probed with anti-CD9 antibody (1:2000, Abcam) followed by detection using goat anti-rabbit IgG-HRP conjugated secondary antibody. The signals were detected using an enhanced chemiluminescent (ECL) kit.