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Particle size was determined by optical microscopy using optical trianocular microscope coupled with a camera at 100× objective.
There was no absorption by pyrene at the scattering wavelengths so the average index of refraction was determined by optical microscopy using index matching fluids (Cargille catalog #18005).
Prior to mechanical testing the integrated interface area of each sample was determined by optical microscopy using the imaging software analySIS 3.1 (SZX12, Olympus, Hamburg, Germany).
11, 33– 35 Proportions of the different populations of red cells, identified by optical microscopy using Bessis 's morphological index, are presented in Figure 1 for all three pholyphenolic extracts at both concentrations.
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Michaelis, J., Hettich, C., Mlynek, J. & Sandoghdar, V. Optical microscopy using a single-molecule light source.
Delamination damage was assessed by ultrasonics and optical microscopy used to observe intra-laminar mechanisms.
The gold surfaces with thin mica flakes on it were then characterized by optical reflection microscopy using an AxioImager A1m (Zeiss, Oberkochen, Germany) mounted with an AxioCam ERc5s camera.
The particle size of the prepared microcapsules was estimated by optical microscopy and confirmed using a particle size analyzer.
(1) In order to investigate whether alcohol loss and uptake takes place through particular crystal faces, the loss of MeOH from 1-MeOH to form 1-A HT and the uptake of MeOH by 1-A HT to form 1-MeOH was examined by optical microscopy and AFM using single crystals.
The progress of wear was studied by optical microscopy and the used inserts were studied by electron microscopy.
Cell phenotype was studied by optical microscopy and indirect immunofluorescence, using smooth muscle α-actin, desmin and SM-Myosin Heavy Chain (SM-MHC) antibodies.
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