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Fig. 1 | Molecular Cancer

Fig. 1

From: Transcriptome reprogramming by cancer exosomes: identification of novel molecular targets in matrix and immune modulation

Fig. 1

Physical characterisation of exosomal size and concentrations. a scanning electron microscopy at low magnification (left panel) and a subset showing high magnification (right panel) showing approximate diameters of each particle. b Transmission electron microscopy at low magnification (left panel) and a subset showing high magnification (right panel), note the arrows indicating lipid-bilayer membrane structure. c Zetasizer measurements on exosomes (Exo), microvesicles (MV) and cell debris (CD) fractions of two cell lines SVpgC2a and SVFN8. d NanoSight particle analysis on exosomes derived from 3 normal primary human oral keratinocytes (OK113, NK4 and NOK368) and 5 malignant (Ca1, CaLH2, SqCC/Y1, SVpgC2a and SVFN8) HNSCC cell lines. Numbers indicated within the diagram indicates the peak size (nm)

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