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Film morphology was monitored with Brewster Angle Microscopy.
Cells were transfected with small interfering RNAs (siRNAs) (Figure 3a), transferred into the Matrigel and organoid morphology was monitored for 8 days.
In the experiments, flocs were formed in a standard mixing apparatus and their morphology was monitored by using a microscope.
Temporal variation of intertidal-channel morphology was monitored using a RTK GPS over three years in the macrotidal embayment of Gomso Bay, west coast of Korea.
During their growth on the polymers, the evolution of the cell morphology was monitored using both confocal microscopy and immunohistochemistry, leading to the conclusion of a normal development.
Cell morphology was monitored with a phase-contrast microscope (IX71; Olympus, Tokyo, Japan).
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Alterations in protein secretion, intracellular signaling, and cell morphology were monitored; and the role of integrin signaling in MSeA-induced morphological alterations was investigated using divalent cation treatments.
Structural morphology is monitored in situ during monolayer dissolution and reassembly within the thin liquid wetting film.
ApoA-I induced changes in ABLC solubility and morphology were monitored by spectroscopy and electron microscopy.
Porosity variations and morphology were monitored using N2 adsorption and helium pycnometry.
Microstructural changes following thermal annealing of films with cylindrical and lamellar morphology were monitored using two-dimensional small angle X-ray scattering, transmission electron microscopy and thermomechanical analysis.
More suggestions(15)
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