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. Author manuscript; available in PMC: 2021 Aug 11.
Published in final edited form as: J Vis Exp. 2018 Nov 9;(141):10.3791/58310. doi: 10.3791/58310

Table 2: The ultrafiltration centrifugation isolation method provided a high murine bronchoalveolar lavage fluid-derived extracellular vesicle yield.

The particle concentration and total particle count were measured by nanoparticle tracking analysis (NTA). The protein concentration and total amount of protein were measured by a bicinchoninic acid protein assay.

Methods Starting Volume (mL) NTA* (x108/μL) Total Particles (x1010) Protein Conc (μg/μL) Total Proteins§ (μg)
UFC 35 7.69 ± 2.6 29.4 ± 18.4 3.7 3,136 ± 1860
UC-DGC 35 0.5 ± 0.05 0.5 ± 0.1 0.6 73.7 ± 38.3
*

BALF EVs’ particle concentration (mean ± SEM x 108/μL from three independent experiments).

BALF EVs’ total particle (mean ± SEM x 1010 particles from three independent experiments).

BALF EVs’ protein concentration (mean ± SEM μg/μL from three independent experiments).

§

BALF EVs’ total protein (mean ± SEM mg from three independent experiments).

UFC: ultrafiltration centrifugation; UC-DGC: ultracentrifugation with density gradient centrifugation; Conc: concentration; NTA: nanoparticle tracking analysis; SEM: standard error of the mean.