Can you explain more about the slide in 21:27? The count check beads are added to determine EVs number, so beads do not bind to EVs? I meant why beads are at the position 10^3. And how to you identify EVs size distribution through FSC and SSC? I’m really looking forward to your response, thanks so much
Great question! Bio-Techne recommends you join the CCMA Session on Small Particle Flow Cytometry - Wed. Feb 17, 2021 @ noon ET. Register to learn about the latest advances in phenotypic analysis of small particles such as extracellular vesicles and viruses from the experts on small particle flow cytometry. docs.google.com/forms/d/e/1FAIpQLScBJd425mf80dee8dAfFYnuP8G_Xm7kQ4b1tOXT1vGFQiShPg/viewform
![[Exosome] Exosome Maximum Production Kit를 이용한 초고속 Extracellular Vesicles (EVs) 대량 생산 방법](http://i.ytimg.com/vi/v0tSlBHUbJY/mqdefault.jpg)
Can you explain more about the slide in 21:27? The count check beads are added to determine EVs number, so beads do not bind to EVs? I meant why beads are at the position 10^3. And how to you identify EVs size distribution through FSC and SSC? I’m really looking forward to your response, thanks so much
Great question! Bio-Techne recommends you join the CCMA Session on Small Particle Flow Cytometry - Wed. Feb 17, 2021 @ noon ET. Register to learn about the latest advances in phenotypic analysis of small particles such as extracellular vesicles and viruses from the experts on small particle flow cytometry. docs.google.com/forms/d/e/1FAIpQLScBJd425mf80dee8dAfFYnuP8G_Xm7kQ4b1tOXT1vGFQiShPg/viewform