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Inset: pore size distribution.

For motility assay, 1 × 10 cells were plated on the top chamber of a non-coated polyethylene teraphthalate membrane (six-well inset, pore size 8  μm; Becton Dickinson, Franklin Lakes, NJ, USA).

Inset BJH pore size distribution derived from the N2 sorption isotherms.

D N2 adsorption-desorption isotherms of Sep and SnO2 C@Sep; the inset shows pore diameter distributions obtained by analysis of N2 adsorption Fig. 3 SEM images of a, b raw sepiolite and c, d SnO2 C@Sep Fig. 4 TEM images of a, b raw sepiolite and c, d SnO2 C@Sep.

Scale bars in the FE-SEM and FE-TEM images are 2 μm and 10 nm, respectively Fig. 2 a Raman spectra, b XRD patterns, c XPS C 1s spectra, and d nitrogen adsorption and desorption isotherm curves (inset of pore size distribution data) of HM-CNWs and HM-GNWs.

Insets: the pore size distribution of the crystals.

Inset: the pore-size distribution calculated based on the desorption branch of the corresponding isotherm.

MDCK cells expressing human CXCR7, CXCR7-DRYLAIV, CXCR4, mock-transfected MDCK, or primary HUVECs were grown on Transwell® insets (Costar, pore size 8 µm).

Inset depicts the pore size distributions of samples.

The inset shows the pore size distribution of the MWCNTs/GO and PDDA-MWCNTs/GO membranes.

The inset shows the pore size distributions of the different samples.