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transmission electron microscope philips em 208 s  (Philips Healthcare)

 
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    Philips Healthcare transmission electron microscope philips em 208 s
    Transmission Electron Microscope Philips Em 208 S, supplied by Philips Healthcare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/208+s+transmission+electron+microscope/scanning+electron+microscope+philips+xl30/10__1016_slash_j__colsurfa__2024__134473-70-37-33
    Average 90 stars, based on 1 article reviews
    transmission electron microscope philips em 208 s - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Transmission Assay:

    Article Title: Persistent immunogenicity of integrase defective lentiviral vectors delivering membrane-tethered native-like HIV-1 envelope trimers.
    Article Snippet: .. Sections were observed with a Philips 208 S transmission electron microscope at 100 kV. ..

    Article Title: Aerenchyma formation in the rice stem and its promotion by H2O2.
    Article Snippet: • Gas spaces (aerenchyma) form as an adaptation to submergence to facilitate gas exchange.. In rice (Oryza sativa), aerenchyma develop by cell death and lysis, which are poorly understood at the cellular level.. • Aerenchyma formation was studied in rice stems by light microscopy.

    Article Title: IL-33 stimulates the anticancer activities of eosinophils through extracellular vesicle-driven reprogramming of tumor cells
    Article Snippet: Cells were then dehydrated in ethanol gradient from 50 to 100% (v/v) and embedded in Agar 100 resin (Agar Scientific) at 65°C for 48 h. Ultrathin sections were obtained by an ultra-microtome and collected on 200-mesh grids, counterstained with uranyl acetate for 10 min and lead citrate for further 10 min. .. Samples were observed in a Philips 208 s transmission electron microscope at 100 kW (Philips). ..

    Microscopy:

    Article Title: Persistent immunogenicity of integrase defective lentiviral vectors delivering membrane-tethered native-like HIV-1 envelope trimers.
    Article Snippet: .. Sections were observed with a Philips 208 S transmission electron microscope at 100 kV. ..

    Article Title: Aerenchyma formation in the rice stem and its promotion by H2O2.
    Article Snippet: • Gas spaces (aerenchyma) form as an adaptation to submergence to facilitate gas exchange.. In rice (Oryza sativa), aerenchyma develop by cell death and lysis, which are poorly understood at the cellular level.. • Aerenchyma formation was studied in rice stems by light microscopy.

    Article Title: IL-33 stimulates the anticancer activities of eosinophils through extracellular vesicle-driven reprogramming of tumor cells
    Article Snippet: Cells were then dehydrated in ethanol gradient from 50 to 100% (v/v) and embedded in Agar 100 resin (Agar Scientific) at 65°C for 48 h. Ultrathin sections were obtained by an ultra-microtome and collected on 200-mesh grids, counterstained with uranyl acetate for 10 min and lead citrate for further 10 min. .. Samples were observed in a Philips 208 s transmission electron microscope at 100 kW (Philips). ..

    Transmission Electron Microscopy:

    Article Title: Aerenchyma formation in the rice stem and its promotion by H2O2.
    Article Snippet: • Gas spaces (aerenchyma) form as an adaptation to submergence to facilitate gas exchange.. In rice (Oryza sativa), aerenchyma develop by cell death and lysis, which are poorly understood at the cellular level.. • Aerenchyma formation was studied in rice stems by light microscopy.



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    transmission electron microscope philips em 208 s  (Philips Healthcare)
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    Philips Healthcare transmission electron microscope philips em 208 s
    Transmission Electron Microscope Philips Em 208 S, supplied by Philips Healthcare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/208+s+transmission+electron+microscope/scanning+electron+microscope+philips+xl30/10__1016_slash_j__colsurfa__2024__134473-70-37-33
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    em 208 s transmission electron microscope  (Philips Healthcare)
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    Detection of apoptosis by TUNEL assay. The cell monolayer exposed to K. pneumoniae -OMV (50 μg) and LPS (50 μg) for 14 h was fixed with 4 % paraformaldehyde and permeabilized with 0.25 % Triton-X 100. DNA fragmentation was detected through labeling of the 3′-OH terminals with EdUTP, mediated by the TdT enzyme. Images were acquired using the TCS SP5 laser scanning confocal <t>microscope</t> at 20 × magnification, with a 2.5× zoom of a representative field. The unexposed cells (CTRL negative) showed regular nuclei and uniform blue staining of the chromatin, while the cells treated with purified vesicles and LPS were TUNEL positive, recording an intense red staining. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Detection of apoptosis by TUNEL assay. The cell monolayer exposed to K. pneumoniae -OMV (50 μg) and LPS (50 μg) for 14 h was fixed with 4 % paraformaldehyde and permeabilized with 0.25 % Triton-X 100. DNA fragmentation was detected through labeling of the 3′-OH terminals with EdUTP, mediated by the TdT enzyme. Images were acquired using the TCS SP5 laser scanning confocal <t>microscope</t> at 20 × magnification, with a 2.5× zoom of a representative field. The unexposed cells (CTRL negative) showed regular nuclei and uniform blue staining of the chromatin, while the cells treated with purified vesicles and LPS were TUNEL positive, recording an intense red staining. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Detection of apoptosis by TUNEL assay. The cell monolayer exposed to K. pneumoniae -OMV (50 μg) and LPS (50 μg) for 14 h was fixed with 4 % paraformaldehyde and permeabilized with 0.25 % Triton-X 100. DNA fragmentation was detected through labeling of the 3′-OH terminals with EdUTP, mediated by the TdT enzyme. Images were acquired using the TCS SP5 laser scanning confocal <t>microscope</t> at 20 × magnification, with a 2.5× zoom of a representative field. The unexposed cells (CTRL negative) showed regular nuclei and uniform blue staining of the chromatin, while the cells treated with purified vesicles and LPS were TUNEL positive, recording an intense red staining. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    transmission electron microscope tem philips em 208 s  (Philips Healthcare)
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    Detection of apoptosis by TUNEL assay. The cell monolayer exposed to K. pneumoniae -OMV (50 μg) and LPS (50 μg) for 14 h was fixed with 4 % paraformaldehyde and permeabilized with 0.25 % Triton-X 100. DNA fragmentation was detected through labeling of the 3′-OH terminals with EdUTP, mediated by the TdT enzyme. Images were acquired using the TCS SP5 laser scanning confocal <t>microscope</t> at 20 × magnification, with a 2.5× zoom of a representative field. The unexposed cells (CTRL negative) showed regular nuclei and uniform blue staining of the chromatin, while the cells treated with purified vesicles and LPS were TUNEL positive, recording an intense red staining. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Image Search Results


    Detection of apoptosis by TUNEL assay. The cell monolayer exposed to K. pneumoniae -OMV (50 μg) and LPS (50 μg) for 14 h was fixed with 4 % paraformaldehyde and permeabilized with 0.25 % Triton-X 100. DNA fragmentation was detected through labeling of the 3′-OH terminals with EdUTP, mediated by the TdT enzyme. Images were acquired using the TCS SP5 laser scanning confocal microscope at 20 × magnification, with a 2.5× zoom of a representative field. The unexposed cells (CTRL negative) showed regular nuclei and uniform blue staining of the chromatin, while the cells treated with purified vesicles and LPS were TUNEL positive, recording an intense red staining. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Heliyon

    Article Title: Klebsiella pneumoniae -OMVs activate death-signaling pathways in Human Bronchial Epithelial Host Cells (BEAS-2B)

    doi: 10.1016/j.heliyon.2024.e29017

    Figure Lengend Snippet: Detection of apoptosis by TUNEL assay. The cell monolayer exposed to K. pneumoniae -OMV (50 μg) and LPS (50 μg) for 14 h was fixed with 4 % paraformaldehyde and permeabilized with 0.25 % Triton-X 100. DNA fragmentation was detected through labeling of the 3′-OH terminals with EdUTP, mediated by the TdT enzyme. Images were acquired using the TCS SP5 laser scanning confocal microscope at 20 × magnification, with a 2.5× zoom of a representative field. The unexposed cells (CTRL negative) showed regular nuclei and uniform blue staining of the chromatin, while the cells treated with purified vesicles and LPS were TUNEL positive, recording an intense red staining. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: TEM images were acquired using an EM 208 S transmission electron microscope (Philips, Amsterdam, Netherlands).

    Techniques: TUNEL Assay, Labeling, Microscopy, Staining, Purification