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tem micrographs  (JEOL)


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    JEOL tem micrographs
    Tem Micrographs, supplied by JEOL, used in various techniques. Bioz Stars score: 99/100, based on 13799 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tem+micrographs/JEM-F200+Transmission+Electron+Microscope/pm41545451-213-0-6
    Average 99 stars, based on 13799 article reviews
    tem micrographs - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Transmission Electron Microscopy:

    Article Title: Local Microstructural Environments Govern Evolution of Precipitate-Dislocation Interactions in an Al-Sc Alloy: Plasticity Regulation and Crack-Path Selection.
    Article Snippet: .. The electrolyte consisted of 10% perchloric acid and 90% ethanol, and electropolishing was performed at −30 ◦C under an applied voltage of 20 V. In-situ TEM tensile experiments were conducted using a JEM-F200 transmission electron microscope (JEOL Ltd., Akishima, Tokyo, Japan) operated at an accelerating voltage of 200 kV. .. Tensile loading was applied using a Gatan 671 single-tilt liquid-nitrogen cooling tensile holder (Gatan, Inc., Warrendale, USA) at a constant displacement rate of 2.0 μm s−1.

    Transmission Assay:

    Article Title: Local Microstructural Environments Govern Evolution of Precipitate-Dislocation Interactions in an Al-Sc Alloy: Plasticity Regulation and Crack-Path Selection.
    Article Snippet: .. The electrolyte consisted of 10% perchloric acid and 90% ethanol, and electropolishing was performed at −30 ◦C under an applied voltage of 20 V. In-situ TEM tensile experiments were conducted using a JEM-F200 transmission electron microscope (JEOL Ltd., Akishima, Tokyo, Japan) operated at an accelerating voltage of 200 kV. .. Tensile loading was applied using a Gatan 671 single-tilt liquid-nitrogen cooling tensile holder (Gatan, Inc., Warrendale, USA) at a constant displacement rate of 2.0 μm s−1.

    Microscopy:

    Article Title: Local Microstructural Environments Govern Evolution of Precipitate-Dislocation Interactions in an Al-Sc Alloy: Plasticity Regulation and Crack-Path Selection.
    Article Snippet: .. The electrolyte consisted of 10% perchloric acid and 90% ethanol, and electropolishing was performed at −30 ◦C under an applied voltage of 20 V. In-situ TEM tensile experiments were conducted using a JEM-F200 transmission electron microscope (JEOL Ltd., Akishima, Tokyo, Japan) operated at an accelerating voltage of 200 kV. .. Tensile loading was applied using a Gatan 671 single-tilt liquid-nitrogen cooling tensile holder (Gatan, Inc., Warrendale, USA) at a constant displacement rate of 2.0 μm s−1.

    other:

    Article Title: Disrupting Mitochondrial Homeostasis via TBC1D15 Protein.
    Article Snippet: Morphology and particle size distribution were examined via transmission electron microscopy (TEM, JEM-F200, JEOL Ltd., Akishima, Tokyo, Japan).



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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.
    Tem Micrographs, supplied by JEOL, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tem+micrographs/JEM-F200+Transmission+Electron+Microscope/pm41545451-213-0-6
    Average 99 stars, based on 1 article reviews
    tem micrographs - by Bioz Stars, 2026-11
    99/100 stars
    		  Buy from Supplier

    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