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The mice who raced on the treadmills showed evidence of molecular changes in several portions of their brains when viewed under a microscope, while the voluntary wheel-runners had changes in only one area.
The granules were examined using scanning electron microscope while the green parts were analyzed by green density measurement.
Rapid permittivity measurement on the film libraries was carried out by a scanning microwave microscope, while the crystal structure was by a combinatorial X-ray diffractometer (XRD).
A comparatively uniform distribution of pore in case of foamed concrete with natural sand was observed by scanning electron microscope, while the pores were connected mostly and irregularly for mixes containing a percentage higher than 25% clay brick aggregate.
The surface morphologies were investigated by a field emission scanning electron microscope, while the surface reflectance and wettability were examined by a UV VIS-NIR spectrophotometer and a drop shape analysis system, respectively.
The quantitative analysis for estimating the abundance of protozoans and rotifers was performed with a Sedgwick Rafter chamber and an Olympus CX 31™ compound light microscope, while the crustaceans were enumerated in a 10-ml Bogorov chamber under an Olympus SZ 61™ stereo zoom microscope.
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A dichroic mirror was used to reflect the infrared beam into the microscope while transmitting the visible light onto the CCD (Q Imaging Retiga EXi).
These recent advances in DHM techniques also create unique opportunities to simplify the architecture of conventional bench-top microscopes, while also providing a decent imaging performance over large sample volumes, which is an important need in general for e.g., high-throughput imaging/screening applications.
This was found to be due to the fact that at sufficiently low overpotentials the grain growth becomes inhibited for unknown reason before it becomes visible under the optical microscope, while at high overpotentials the large numbers of nuclei formed, lead to fine-grained compact deposits.
Morin et al. screened first instar larvae manually with a dissecting microscope, while both of the large-scale screens utilised an automated embryo sorter.
Animals were imaged live under a confocal microscope while stained with the vital dye Alizarin red, as described previously [ 44]. Whole-mount and section RNA in situ hybridization were carried out as described [ 41, 48].
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