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Various cellular responses (i.e., cell attachment, viability, and proliferation) of osteoblast-like MG63 cells cultured on an SF membrane were quantified.
The remodeling of actin fibres and the morphological changes of the membrane were quantified by assessing the intensity of the actin fluorescence after conversion of the coloured pixels to greyscale using the Leica QWin image analysis and processing software.
RPE cells that invaded the lower surface of the membrane were quantified by cell counting (320 × magnification).
The upper side of the membrane was wiped with a cotton swab, and the cells that had migrated to the lower side of the membrane were quantified.
The membrane was hybridized with radiolabeled specific DNA probes, and the signals on the membrane were quantified using an image analyzing system, FLA-3000 (Fuji Film Inc. Tokyo).
Cells in the upper chamber were then removed, and cells that had migrated onto the lower surface of the membrane were quantified.
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Weaker adhesion force mapping of the patterned MD membrane was quantified.
The effect of these degradation products on the membrane gas absorption process using PP hollow fiber membrane was quantified.
The optical density (OD) of stress protein bands on the membrane was quantified on digitized images using the software package Image ProPlus.
The number of cells at the lower side of each membrane was quantified by counting of cells from three randomly chosen sections (3.7 mm2) using an Olympus IX 1 fluorescence microscope (Olympus, Planegg, Germany).
The number of cells that had invaded into the matrigel and migrated through the pores of the membrane was quantified for each well with a fluorescence plate reader (excitation 544 nm, emission 590 nm).
More suggestions(15)
membrane were analysed
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surface were quantified
film were quantified
wall were quantified
layer were quantified
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membrane were purified
membrane were visualized
membrane were placed
membrane were removed
membrane were investigated
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