Fig. 4From: Apoptotic bodies: bioactive treasure left behind by the dying cells with robust diagnostic and therapeutic application potentialsDifferential centrifugation for ApoBDs isolation. After induction of apoptosis by UV or staurosporine, the supernatant is centrifuged at 300–400g for 10 min at 4 ℃ to remove the large apoptotic cells and fragments. Then, the supernatant is centrifuged at 1000g–4000g for 15–30 min at 4 ℃ to separate micron-size ApoBDs. At last, nano-size ApoBDs are obtained from precipitate through centrifugation of the supernatant at 16,000g for 30 min at 4 ℃. Created with BioRender.comBack to article page