Abstract
Extracellular vesicles (EVs) are lipid-bound particles that are released by the cells into
the extracellular space. However, the nature of EVs being small, make their analysis
difficult. Flow cytometry is useful tool for analyzing a sample and its use for analyzing
EVs is much desired. To overcome the size limitations, bead-assisted flow cytometry
provides a mean for doing so. Yet, direct EV flow cytometry could potentially produce
other reliable results that the nature of bead-assisted cannot. In this thesis, we studied
four different samples by applying different analysis methods, followed by direct EV
flow cytometry to determine whether it is possible to detect them via this method.