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Microscopic observations were done using trinocular microscope (Carl Zais Axio ImageM2, Germany).
Microscopic observations were done using a dissecting fluorescent microscope SZX12 (Olympus, Japan) and a compound microscope Zeiss Axioscope2.
Microscopic observations were carried out under an epifluorescence microscope (AxioPlan 2 Imaging System, Carl Zeiss, Jena, Germany).
Microscopic observations were taken on an AxioImager M1 microscope equipped with an Axio Cam MRm camera (Carl Zeiss Canada, Toronto, ON, Canada).
All microscopic observations were made on a Zeiss intravital microscope (Axioskop, Carl Zeiss, Inc., Thornwood, NY), with a saline immersion objective (SW 40/0.75 numerical aperture).
In vivo fluorescence microscopic observations were made using confocal laser scanning microscope Leica TCS-SP5, using 488 nm for the fluorescence excitation of Citrine.
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These microscopic observations are used to predict friction using a constant interface shear strength model.
Therefore, quantitative microscopic observations are required to evaluate histopathological alterations objectively.
Polarizing microscopic observations are indicative of highly ordered smectic mesophases, which owe their origin to the hard segments.
The final BacLight solution used for the microscopic observations was freshly prepared by mixing 1.5 μL of both stain stock solutions with 97 μL of distilled water.
Experiments with macroscopic and microscopic observations are used to characterize the material quantitatively and to calibrate the constitutive and damage models.
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