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The presence of grafted poly-DADMAC on the polypropylene surface was confirmed using SEM, FT-IR and TOF-SIMS techniques.
The presence of the peptide on the electrode surface was confirmed using Fourier transform infrared spectroscopy and scanning electron microscopy (SEM).
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Surface characterization was confirmed using the SEM and FT-IR studies.
The surface modification was confirmed using infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), environmental scanning electron microscopy (ESEM), and contact angle measurements.
As shown in Figure 1, the EG surface structure was confirmed using LEED and C 1 s core-level spectroscopy (not shown here) and then immersed into a benzoic acid solution for 3 min. The surface was subsequently reintroduced into the UHV chamber.
Consequently, as released atomic hydrogen facilitates CH adsorption on the surface of nanodiamond which was confirmed using infrared spectroscopy.
The HA layer formation, which is an indicator of the bioactivity on the surface of the R-SBgC, was confirmed using SEM, EDX and further by FTIR.
This was confirmed using surface biotinylation in primary hippocampal cultures (Figure 1F H).
The modification of surface carboxyl and amino groups on FSNPs was confirmed using FT-IR spectroscopy Nicolet-57000, USA).
Cell surface expression of the D50A and T118A mutant receptors was confirmed using a membrane-impermeable biotinylating agent as described elsewhere [1] (data not shown).
First, surface expression of the ephrin type-A receptor 2 (EPHA2) receptor was confirmed using FACS analysis.
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