transmission electron microscopy fixative (Servicebio Inc)
86
Structured Review
Servicebio Inc
transmission electron microscopy fixative

Transmission Electron Microscopy Fixative, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fixed/electron+fixative+microscopy/pmc13264258-296-15-20
Average 86 stars, based on 1 article reviews

Transmission Electron Microscopy Fixative, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fixed/electron+fixative+microscopy/pmc13264258-296-15-20
Average 86 stars, based on 1 article reviews
transmission electron microscopy fixative - by Bioz Stars,
2026-11
86/100 stars
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1) Product Images from "Targeting Rap1-YAP1 mechanosignaling for ameliorating acute IOP elevation-induced trabecular meshwork dysfunction"
Article Title: Targeting Rap1-YAP1 mechanosignaling for ameliorating acute IOP elevation-induced trabecular meshwork dysfunction
Journal: iScience
doi: 10.1016/j.isci.2026.116268
Figure Legend Snippet: Structural evaluation of the mouse TM following acute IOP elevation (A) Photographs reveal that mice underwent direct cannulation of the anterior chamber (AC) in the eye. Eyeballs were harvested immediately after the procedure, and the gross appearance is illustrated in the right. (B) Intraocular pressure (IOP) measurement following acute ocular hypertension. IOP was measured at baseline (0 days), 3 days, and 7 days following 45 mmHg pressure for 1 h. Data represent mean ± SD. two-way ANOVA was used for comparing IOP between control and HIOP groups across time points. Post hoc test: ns, not significant, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001 vs. control group at corresponding time point. N = 9 mice per group. (C) Representative hematoxylin staining of anterior chamber angles 3 days after IOP elevation. Magnification bars: 1 mm. (D) Ultrastructural appearance of the TM tissues by transmission electron microscopy. Leftmost: representative lower magnification image of the TM and SC. Right: higher magnification of the TM cells. The regions encased in black boxes are magnified. TM, trabecular meshwork; SC, Schlemm’s canal; red arrow indicates giant vacuoles.
Techniques Used: Control, Staining, Transmission Assay, Electron Microscopy
Figure Legend Snippet: Pathological changes in HTM cells under high hydrostatic pressure (A and B) Representative examples of human trabecular meshwork (HTM) cells cultured under control (con) or high hydrostatic pressure for 12 h, 1 day (1 D), and 3 days (3 D) immunolabeled for EDU (A) and TUNEL (B) assay. Scale bars, 50 μm. Bar graphs summarizing the effects of high hydrostatic pressure on the proliferation and death of HTM cells. N = 3. Magnification bars, 100 μm. (C) Histological evaluation of different groups of HTM cells by transmission electron microscopy. N = 3. Magnification bars, 50, 10, and 2 μm from the left to the right. (D) Representative fluorescence micrographs of F-actin in HTMs subjected to 12 h, 1D, and 3D culture under high hydrostatic pressure and the control, with nuclei and F-actin labeling shown in blue and green, respectively. The asterisk indicates cross-linked actin network (CLAN+) cells and the percentage of CLAN+ cells was analyzed. N = 5. Magnification bars, 25 μm. (E) Expression of fibronectin, collagen I and α-SMA in the different groups of HTM cells by western blots. N = 6. ns, not significant, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001. Data represent mean ± SD.
Techniques Used: Cell Culture, Control, Immunolabeling, TUNEL Assay, Transmission Assay, Electron Microscopy, Fluorescence, Labeling, Expressing, Western Blot
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