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ABSTRACT: Background
Exosomes are nanovesicles (30-120 nm) of endosomal origin. These exosomes contain various functional proteins and RNAs that could be used for therapeutic purposes. Currently, having a standard method for exosome isolation retaining its biological properties with increased yield and purity is a major challenge. The most commonly used method is differential ultracentrifugation but it has its own disadvantages, which include high time consumption, low yield due to disruption of exosome integrity, and high protein contaminants. In this study, we have identified an improved method addressing these problems for exosome isolation using ultracentrifugation since it is cost-effective and used worldwide.Method
We have compared differential ultracentrifugation with the modi
SUBMITTER: Gupta S
PROVIDER: S-EPMC6033286 | biostudies-literature | 2018 Jul
REPOSITORIES: biostudies-literature