Creative Proteomics can efficiently separate high-quality exosomes derived from multiple cell types, such as B cells, dendritic cells and tumor cells and almost any biofluid including plasma, urine, serum, CSF, ascites fluid, and saliva, as well as plants.

We uses different exosome isolation methods including differential ultracentrifugation, size-based isolation of exosomes, exosome precipitation, affinity-based capture of exosome, microfluidics-based isolation of exosome according to customer's detailed requirements.

  • The isolation of exosomes by differential ultracentrifugation usually consists of a series of centrifugation cycles of different centrifugal force and duration to isolate exosomes based on their density and size differences from other components in a sample;
  • Before the start of isolation, a cleaning step is usually carried out for human plasma/serum to rid of large bioparticles in a sample and the sample is spiked with protease inhibitors to prevent the degradation of exosomal proteins;
  • Finally, the isolated exosomes are once again re-suspended and stored at -80℃ until further analysis.

Mitochondrial Isolation
Fig1. Schematic representation of isolating exosomes by differential ultracentrifugation (Li P.; et.al, 2017)

Creative Proteomics promises to provide high-quality and low-cost exosomes for global clients. We also believe that our service will make your project achieve twice the result with half the effort. If you have any demands in exosome isolation, please don't hesitate to contact us for more information.