Research Paper Volume 13, Issue 6 pp 8467—8480

Determining the influence of high glucose on exosomal lncRNAs, mRNAs, circRNAs and miRNAs derived from human renal tubular epithelial cells

The identification of exosomes. Representative TEM image of exosomes derived from two groups (A). Western blot of the exosomal markers CD63, CD9, and CD81 and non-exosomal protein markers β-Actin in exosomes and monocytes (B). The size of the exosomes (nm) enriched from the culture supernatant of two groups was examined through NTA using a NanoSight NS300 instrument (NanoSight Ltd., Amesbury, UK) (C).

Figure 1. The identification of exosomes. Representative TEM image of exosomes derived from two groups (A). Western blot of the exosomal markers CD63, CD9, and CD81 and non-exosomal protein markers β-Actin in exosomes and monocytes (B). The size of the exosomes (nm) enriched from the culture supernatant of two groups was examined through NTA using a NanoSight NS300 instrument (NanoSight Ltd., Amesbury, UK) (C).