Fig. 32.1 (a) A schematic representation of “in vivo cryotechnique ” (IVCT) for the mouse cerebellum after opening the scull; cryoknife is push into the cerebellum and simultaneously isopentane –propane…
Fig. 15.1 Morphological features of mouse lungs. (a, c) Macroscopic images of normal mouse lungs under experimental expiration (Ex) and inspiration (In). (b, d) Light microscopic images with HE staining…
Fig. 30.1 (a–d) Light micrographs of HE-staining (a, c) and immunostaining for albumin (b, d) in seminiferous tubules of the normal (a, b) and the 24 h cadmium -treated (c,…
Fig. 27.1 (a, b) Representative electron micrographs of the apical cytoplasm of umbrella cells in mouse bladder under the absence (a; Normal) and presence (b; Dynasore) of the dynasore treatment….
Fig. 8.1 Light micrographs of HE staining (HE; a, b), immunostaining for IgA (c), Igκ (d), IgG1 (e), and IgM (f), confocal laser scanning micrographs of double-fluorescence immunostaining for IgA…
Fig. 10.1 Light micrographs of hematoxylin-eosin (HE) staining for paraffin sections of mesenteric lymph nodes prepared by IVCT followed by FS fixation. (a) Lower magnified view of a lymph node…
Fig. 12.1 Scanning electron micrographs of flowing erythrocyte s in abdominal aorta (a) and inferior vena cava (c) of living mice, in addition to both images reconstructed by serial ultrathin…
Fig. 6.1 Three-dimensional reconstruction of triple-fluorescence images obtained by confocal laser scanning microscopy with PAS staining (red), immunostaining for immunoglobulin kappa light chain (green), and TO-PR-O3 (blue) in fasting mouse…
Fig. 16.1 Light (a) and electron (b–d) micrographs of pleural and pulmonary structures of inflating lungs of living mice, as prepared by the “in vivo cryotechnique ”. In the light…
Fig. 13.1 Electron micrographs of intestinal smooth muscle cell s in normal scn mice (a, b) and dystrophin-deficient mdx mice (c, d). They were prepared by the “in vivo cryotechnique…
