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The accumulation of the drugs on the modified electrode surface was ascertained by carrying out SEM analysis.
β1AR specificity of IgG signals thus obtained on the cell surface was ascertained by their absence upon the omission of first antibody, pre-adsorption with a 1000-fold molar excess of a peptide homologue of the second extracellular loop of the human β1AR or in cells not overexpressing the β1AR or overexpressing GFP-fused human EGF receptors instead.
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The surface composition of deposits was ascertained by chemical analysis (WDXRF).
The binding affinity of the peptide for VEGF165 was ascertained by surface plasmon resonance and compared with the heparin mimic suramin; the peptide binds to VEGF165 100-fold stronger than the sulfonated compound.
The usefulness of the downsized system was ascertained by analyzing a set of surface water.
Purity of isolated monocytes was ascertained by FSC-SSC parameters and surface expression of CD14 by flow cytometry (FACS Calibur BD Biosciences, San Jose, CA, USA).
The purity of the compounds was ascertained by NMR, differential scanning calorimetry and determination of cmc by surface tension.
Lipoperoxidation was ascertained by the formation of MDA.
The stoichiometric composition of the films was ascertained by X-ray photoelectron spectroscopy.
The assignment of the DMTA transitions was ascertained by varying the gelatin/amylopectin ratio.
Furthermore, the estimated crystallinity was ascertained by the X-ray diffraction experiment.
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CEO of Professional Science Editing for Scientists @ prosciediting.com