fig2

Choice of size-exclusion chromatography column affects recovery, purity, and miRNA cargo analysis of extracellular vesicles from human plasma

Figure 2. The purity of EVs* in the pooled SEC fractions, compared to ApoA1 (HDL) by ELISA (A), ApoB [(V)LDL and chylomicrons] by ELISA (B), and protein as measured by Bradford Assay (C). Experiments were performed in triplicate using pooled plasma obtained from healthy controls. Adjusted P-values (one-way ANOVA with Tukey’s multiple comparisons test) obtained from assessing the statistical differences in EV purity between SEC columns can be found in Supplementary Table 1. A P-value ≤ 0.05 was considered significant, and has been indicated with asterisks in the figure (*P <0.05; **P < 0.01). *EVs were measured using flow cytometry (Apogee A60-Micro) and the concentration of EVs is calculated as the sum of particles that were positively labeled for CD61, CD235a, or CD45, with a size range of 200-650 nm and a refractive index < 1.42; DMC: dual-mode chromatography; EV: extracellular vesicle; SEC2B: size-exclusion chromatography 2B; SEC4B: size-exclusion chromatography 4B.

Extracellular Vesicles and Circulating Nucleic Acids
ISSN 2767-6641 (Online)
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