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Particulates trapped within the film were visualized.
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With a black and white camera the hydrodynamics of the moving film is visualized, whereas the temperature field below the foil is qualitatively measured with an IR camera.
Also the surface properties of PEI/TiO2 thin films were visualized using an atomic force microscope (Mobile S, Nanosurf, Switzerland).
The expression levels of E-selectin, VCAM, CD146, and VE-cadherin on the EC surface for the two collagen films were visualized using immunostaining method and confocal imaging technique.
The growth of highly conductive nanodomains in regioregular poly 3-hexylthiophene) (poly 3-hexylthiophenevisualized with a resolution of 20 nm by conductive atomic force microscoP3HTC-AFM).
The same photochemistry was applied to create NGF patterns on chitosan films which were visualized by immunostaining, and the immobilized NGF remained bioactive as demonstrated with a neuron survival assay.
The membranes were exposed to film and signals were visualized and quantitated using GelPro software.
The membrane was treated with enhanced chemiluminescence detection reagents (Amersham) for 1 min at room temperature and exposed to scientific imaging films (Eastman Kodak), and proteins were visualized as bands.
DNA bands were visualized using Fuji film LAS-3000 (film film, Tokyo, Japan) under ultraviolet transillumination.
The bands were visualized using film exposure with ECL reagent.
The bands were visualized on film (Kodak) exposed to the membrane to detect chemiluminescence signals.
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