Review




Structured Review

Servicebio Inc transmission electron microscopy fixative
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 <t>microscopy.</t> 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.
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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

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.
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

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.
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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Microscopy:

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Dissection:

Article Title: Targeting Rap1-YAP1 mechanosignaling for ameliorating acute IOP elevation-induced trabecular meshwork dysfunction
Article Snippet: IOP was measured in a masked manner using a handheld tonometer (Tonolab; Icare Finland Oy, Vantaa, Finland), with each measurement repeated five times. .. Following dissection, the TM or HTM cells grown on coverslips were immediately immersed in fresh transmission electron microscopy fixative (G1102; Servicebio, Wuhan, China) for 48 h. The samples then underwent post-fixation in a 1% OsO 4 aqueous solution for 2 h at room temperature. .. The samples were subsequently washed, dehydrated, embedded in Polybed 812 resin (90529-77-4; SPI Supplies, West Chester, PA, USA), and observed on a transmission electron microscope (HT7800, Hitachi High-Tech, Tokyo, Japan).

Transmission Assay:

Article Title: Targeting Rap1-YAP1 mechanosignaling for ameliorating acute IOP elevation-induced trabecular meshwork dysfunction
Article Snippet: IOP was measured in a masked manner using a handheld tonometer (Tonolab; Icare Finland Oy, Vantaa, Finland), with each measurement repeated five times. .. Following dissection, the TM or HTM cells grown on coverslips were immediately immersed in fresh transmission electron microscopy fixative (G1102; Servicebio, Wuhan, China) for 48 h. The samples then underwent post-fixation in a 1% OsO 4 aqueous solution for 2 h at room temperature. .. The samples were subsequently washed, dehydrated, embedded in Polybed 812 resin (90529-77-4; SPI Supplies, West Chester, PA, USA), and observed on a transmission electron microscope (HT7800, Hitachi High-Tech, Tokyo, Japan).

Saline:

Article Title: Green tea catechin EGCG attenuates hippocampal atrophy and cognitive impairment in obesity via autophagy signaling.
Article Snippet: .. For electron microscopic analysis, mice were deeply anesthetized with sodium pentobarbital (i.p.) and transcardially perfused with icecold saline, followed by electron microscopy-grade fixative (G1102, Wuhan Servicebio AR TI CL E IN P RE SS Technology Co., Ltd.). ..



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Image Search Results


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Article Title: Sleep deprivation impairs ventral hippocampus-medial prefrontal connectivity and task learning in rats

doi: 10.1016/j.isci.2026.115683

Figure Lengend Snippet:

Article Snippet: Optical microscope , Olympus , BX51WI.

Techniques: Recombinant, Software, Functional Assay, Imaging, Microscopy