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To examine NMJ morphology, we visualized presynaptic motor neurons with the anti-HRP antibody to label neuronal membranes.
To observe detailed cell morphology, we visualized cultured PGCs (Fig. 3A 3B), PGCs purified from the blood of stage 14 17 embryos (Fig. 3C) and the gonad of stage 28 embryos (Fig. 3D) by scanning electron microscopy.
Therefore, we described our optimized method for reduction of CO2 to high-quality uniform AMS targets whose morphology we visualized using scanning electron microscope pictures.
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To visualize bouton morphology, we co-stained with Eps15, a presynaptic marker (Koh et al., 2007) and Dlg1, a postsynaptic marker (Parnas et al., 2001).
To visualize cone morphology, we generated a transgenic line Tg(Trβ2 tdTomato) expressing tdTomato in the long-wavelength cones (this paper and Suzuki et al., in preparation).
In order to visualize the cell morphology, we applied an ANN to analyse the Raman xy-scans of whole single cells.
Therefore, we visualized the morphology of cell organelles, e.g. the cell nucleus by applying k-means cluster analysis and an ANN.
In the present study, we combined 2 histological analyses to examine this relationship: 1) Measurement of spines of neurons whose morphology was visualized in brain sections of mice expressing membrane-targeted green florescent protein (Thy1-mGFP mice) and 2) Categorization of CA1 neurons by immunohistochemical monitoring of Arc expression as a putative marker of recent neuronal activity.
Morphology was visualized by scanning electron microscopy.
Particles with a herpesvirus morphology were visualized in liver tissue.
Most TGs displayed qualitatively good morphology as visualized with Htx-Eosin staining (Figs. 2a f).
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