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scanning electron micrograph  (Hitachi Ltd)


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    Structured Review

    Hitachi Ltd scanning electron micrograph
    Scanning Electron Micrograph, supplied by Hitachi Ltd, used in various techniques. Bioz Stars score: 99/100, based on 20547 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/electron+micrographs/TM4000/pmc13162467-155-7-11
    Average 99 stars, based on 20547 article reviews
    scanning electron micrograph - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Microscopy:

    Article Title: Differential vasoproliferative traits of Bartonella henselae strains associated with autotransporter BafA variants
    Article Snippet: .. Electron micrographs were obtained with the S-4800 field emission scanning electron microscope (Hitachi, Tokyo, Japan). ..

    Article Title: Aldehyde metabolism governs resilience of mucociliary clearance to air pollution exposure
    Article Snippet: .. Electron micrographs were captured with an S-4800 field emission scanning electron microscope (Hitachi High-Technologies Corp.). .. Mucociliary transport was analyzed using fluorescent beads (Fluoresbrite, 0.5 μm; Polysciences) as described previously ( ).

    Article Title: Synergistic Anti‐Aging Effects of Adipose‐Derived Stem Cell Extracellular Vesicles Loaded With Natural Compounds
    Article Snippet: Compounds used in the study included nicotinamide riboside (NR), resveratrol (RES), vitamin C (VITC), retinol (RET) and arbutin (ARB) (Sigma‐Aldrich, Germany). .. Loading efficiencies of RES and ARB were quantified by their fluorescence intensity as measured by the Varioskan Lux (Thermo Scientific, USA) [ ]. sEVs before and after loading were fixed with 4% paraformaldehyde; scanning electron micrographs (SEM) were then obtained using the FESEM SU8010 microscope (Hitachi High‐Technologies, Japan). .. Immunocapture of CD81‐, CD9‐ and CD63‐positive sEVs was performed using the Leprechaun Human Tetraspanin Kit (Unchained Labs, UK) following the manufacturer's protocol.

    Article Title: Nanoformulation, characterization, and biological activity assays of extracts of Derris trifoliata Lour, a rutin-rich mangrove plant
    Article Snippet: .. The electron micrographs were taken by a Hitachi HT 7800 transmission electron microscope (Hitachi, Ltd., Tokyo, Japan) at 80 kV. .. The viscosity of formulated DTE-NE was measured using a Brookfield “DV2T-LV” viscometer (Brookfield, Ametek, DKSH Technology Limited, Bangkok, Thailand) with an LV-1 spindle at 25 ◦C.

    Fluorescence:

    Article Title: Synergistic Anti‐Aging Effects of Adipose‐Derived Stem Cell Extracellular Vesicles Loaded With Natural Compounds
    Article Snippet: Compounds used in the study included nicotinamide riboside (NR), resveratrol (RES), vitamin C (VITC), retinol (RET) and arbutin (ARB) (Sigma‐Aldrich, Germany). .. Loading efficiencies of RES and ARB were quantified by their fluorescence intensity as measured by the Varioskan Lux (Thermo Scientific, USA) [ ]. sEVs before and after loading were fixed with 4% paraformaldehyde; scanning electron micrographs (SEM) were then obtained using the FESEM SU8010 microscope (Hitachi High‐Technologies, Japan). .. Immunocapture of CD81‐, CD9‐ and CD63‐positive sEVs was performed using the Leprechaun Human Tetraspanin Kit (Unchained Labs, UK) following the manufacturer's protocol.

    Transmission Assay:

    Article Title: Nanoformulation, characterization, and biological activity assays of extracts of Derris trifoliata Lour, a rutin-rich mangrove plant
    Article Snippet: .. The electron micrographs were taken by a Hitachi HT 7800 transmission electron microscope (Hitachi, Ltd., Tokyo, Japan) at 80 kV. .. The viscosity of formulated DTE-NE was measured using a Brookfield “DV2T-LV” viscometer (Brookfield, Ametek, DKSH Technology Limited, Bangkok, Thailand) with an LV-1 spindle at 25 ◦C.



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    Characterization and ATX-scavenging activity of AS-Lipo@R. <t>(A)</t> <t>Cryo-TEM</t> images of Lipo and AS-Lipo (scale bar, 100 nm). (B) Particle size and zeta potential of Lipo and AS-Lipo measured by DLS. (C) Colloidal stability of Lipo and AS-Lipo was evaluated by monitoring changes in particle size and zeta potential over 72 h in PBS using DLS. (D) Concentration-dependent inhibition of recombinant mouse ATX activity as a function of BMP-22 concentration in free BMP-22, Lipo, and AS-Lipo, evaluated using a choline release assay. (E) ATX binding to the surface of Lipo and AS-Lipo as a function of ATX concentration, quantified by ELISA. (F) HPLC chromatograms showing rapamycin (R) encapsulation in AS-Lipo@R, as indicated by the disappearance of the free R peak. (G) Cumulative release profiles of rapamycin from Lipo@R and AS-Lipo@R in PBS over 72 h measured by HPLC. (H) Fluorescence imaging showing colocalization of DiO-labeled Lipo or AS-Lipo (green), Alexa Fluor 647 (AF647)-labeled ATX (red), and LysoTracker (purple) in RAW 264.7 macrophages. AS-Lipo-bound ATX is internalized and colocalizes with lysosomes, indicating lysosomal degradation. Right panels show fluorescence intensity profiles along the indicated lines, quantifying the colocalization (scale bar, 100 and 50 μm). Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test ( n = 3). * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001.
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    Image Search Results


    Characterization and ATX-scavenging activity of AS-Lipo@R. (A) Cryo-TEM images of Lipo and AS-Lipo (scale bar, 100 nm). (B) Particle size and zeta potential of Lipo and AS-Lipo measured by DLS. (C) Colloidal stability of Lipo and AS-Lipo was evaluated by monitoring changes in particle size and zeta potential over 72 h in PBS using DLS. (D) Concentration-dependent inhibition of recombinant mouse ATX activity as a function of BMP-22 concentration in free BMP-22, Lipo, and AS-Lipo, evaluated using a choline release assay. (E) ATX binding to the surface of Lipo and AS-Lipo as a function of ATX concentration, quantified by ELISA. (F) HPLC chromatograms showing rapamycin (R) encapsulation in AS-Lipo@R, as indicated by the disappearance of the free R peak. (G) Cumulative release profiles of rapamycin from Lipo@R and AS-Lipo@R in PBS over 72 h measured by HPLC. (H) Fluorescence imaging showing colocalization of DiO-labeled Lipo or AS-Lipo (green), Alexa Fluor 647 (AF647)-labeled ATX (red), and LysoTracker (purple) in RAW 264.7 macrophages. AS-Lipo-bound ATX is internalized and colocalizes with lysosomes, indicating lysosomal degradation. Right panels show fluorescence intensity profiles along the indicated lines, quantifying the colocalization (scale bar, 100 and 50 μm). Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test ( n = 3). * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001.

    Journal: Biomaterials Research

    Article Title: Autotaxin-Scavenging Nanoliposomes for Prolonged Colon Retention and Autophagy-Mediated Mucosal Immune Restoration in Colitis

    doi: 10.34133/bmr.0345

    Figure Lengend Snippet: Characterization and ATX-scavenging activity of AS-Lipo@R. (A) Cryo-TEM images of Lipo and AS-Lipo (scale bar, 100 nm). (B) Particle size and zeta potential of Lipo and AS-Lipo measured by DLS. (C) Colloidal stability of Lipo and AS-Lipo was evaluated by monitoring changes in particle size and zeta potential over 72 h in PBS using DLS. (D) Concentration-dependent inhibition of recombinant mouse ATX activity as a function of BMP-22 concentration in free BMP-22, Lipo, and AS-Lipo, evaluated using a choline release assay. (E) ATX binding to the surface of Lipo and AS-Lipo as a function of ATX concentration, quantified by ELISA. (F) HPLC chromatograms showing rapamycin (R) encapsulation in AS-Lipo@R, as indicated by the disappearance of the free R peak. (G) Cumulative release profiles of rapamycin from Lipo@R and AS-Lipo@R in PBS over 72 h measured by HPLC. (H) Fluorescence imaging showing colocalization of DiO-labeled Lipo or AS-Lipo (green), Alexa Fluor 647 (AF647)-labeled ATX (red), and LysoTracker (purple) in RAW 264.7 macrophages. AS-Lipo-bound ATX is internalized and colocalizes with lysosomes, indicating lysosomal degradation. Right panels show fluorescence intensity profiles along the indicated lines, quantifying the colocalization (scale bar, 100 and 50 μm). Statistical significance was determined by one-way ANOVA with Tukey’s post hoc test ( n = 3). * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001.

    Article Snippet: Cryo-TEM micrographs were acquired using a JEM-2100F electron microscope (JEOL, Japan).

    Techniques: Activity Assay, Zeta Potential Analyzer, Concentration Assay, Inhibition, Recombinant, Release Assay, Binding Assay, Enzyme-linked Immunosorbent Assay, Encapsulation, Fluorescence, Imaging, Labeling