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Collected pupae were temporary mounted on microscopic slide and view at magnification up to 100x under a light microscope (Olympus Optical Co. Ltd., Tokyo).
Individual species of plankton were mounted on microscopic slides on a drop of 20% glycerin after staining with eosin or rose bengal.
For microscopic observation, cells were washed five times with PBS solution to remove unbound anti-6His-FITC antibody, then mounted on microscopic slides and was observed by fluorescence microscopy.
Receptor autoradiography was performed on 20-μm-thick cryostat (Microm HM550, Thermo Fisher Scientific, Walldorf, Germany) sections of the tissue samples, mounted on microscopic slides and then stored at −20°C for at least 3 days to improve adhesion of the tissue to the slide.
Lung transverse sections (thickness, 4 μm) were sliced and mounted on microscopic slides.
The membranes were subsequently cut out and mounted on microscopic slides for quantification.
Similar(51)
Proboscides were prepared by separating the two galeae, embedding in glycerine, and mounting on microscopic slides.
Mosquito guts were dissected on microscopic slides in several drops of the solution, mounted on other microscopic slides in a drop of the staining solution and covered with cover slips.
Furthermore, they can be viewed under the microscope without being mounted on a microscopic glass slide.
After washing (4 × 20 min) with PBS-T, larvae were washed in PBS and mounted on a microscopic slide in 80% (v/v) glycerol for microscopic examination.
Sample was prepared by sprinkling the dispersed nanoparticles onto double-sided adhesive carbon conductive tape which was mounted on a microscopic stub of copper.
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