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transmission light microscope axiovert 25  (Carl Zeiss)


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    Carl Zeiss transmission light microscope axiovert 25
    Transmission Light Microscope Axiovert 25, supplied by Carl Zeiss, 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/result/transmission light microscope axiovert 25/product/Carl Zeiss
    Average 90 stars, based on 1 article reviews
    transmission light microscope axiovert 25 - by Bioz Stars, 2026-03
    90/100 stars

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    Schematic representation of the experimental design. AT-1 Cells were injected within the SNs' perineurial sheath of Copenhagen rats. Different groups were recruited for each timepoint. A sham-operated group was also recruited, in all steps, for comparison purposes. Three paths were taken to perform these experiments. The morphological changes of the extracted SNs were photographed ( 1 ). Tissues of the SNs were sliced, stained by H&E, and visualized under light <t>microscope</t> ( 2 ). For the third path, SN-tissues have been taken away using a different protocol, incubated with the primary and then the fluorochrome-tagged-secondary antibody. Fluorescence captured by confocal laser microscope has been further processed, and the measured intensities were statistically analyzed ( 3 ).
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    https://www.bioz.com/result/inverted light microscope axiovert 25/product/Carl Zeiss
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    Average 90 stars, based on 1 article reviews
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    90/100 stars
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    Carl Zeiss inverted transmitted light microscope zeiss axiovert 25
    Schematic representation of the experimental design. AT-1 Cells were injected within the SNs' perineurial sheath of Copenhagen rats. Different groups were recruited for each timepoint. A sham-operated group was also recruited, in all steps, for comparison purposes. Three paths were taken to perform these experiments. The morphological changes of the extracted SNs were photographed ( 1 ). Tissues of the SNs were sliced, stained by H&E, and visualized under light <t>microscope</t> ( 2 ). For the third path, SN-tissues have been taken away using a different protocol, incubated with the primary and then the fluorochrome-tagged-secondary antibody. Fluorescence captured by confocal laser microscope has been further processed, and the measured intensities were statistically analyzed ( 3 ).
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    Schematic representation of the experimental design. AT-1 Cells were injected within the SNs' perineurial sheath of Copenhagen rats. Different groups were recruited for each timepoint. A sham-operated group was also recruited, in all steps, for comparison purposes. Three paths were taken to perform these experiments. The morphological changes of the extracted SNs were photographed ( 1 ). Tissues of the SNs were sliced, stained by H&E, and visualized under light microscope ( 2 ). For the third path, SN-tissues have been taken away using a different protocol, incubated with the primary and then the fluorochrome-tagged-secondary antibody. Fluorescence captured by confocal laser microscope has been further processed, and the measured intensities were statistically analyzed ( 3 ).

    Journal: Heliyon

    Article Title: Tumor microenvironment (Part I): Tissue integrity in a rat model of peripheral neural cancer

    doi: 10.1016/j.heliyon.2024.e33932

    Figure Lengend Snippet: Schematic representation of the experimental design. AT-1 Cells were injected within the SNs' perineurial sheath of Copenhagen rats. Different groups were recruited for each timepoint. A sham-operated group was also recruited, in all steps, for comparison purposes. Three paths were taken to perform these experiments. The morphological changes of the extracted SNs were photographed ( 1 ). Tissues of the SNs were sliced, stained by H&E, and visualized under light microscope ( 2 ). For the third path, SN-tissues have been taken away using a different protocol, incubated with the primary and then the fluorochrome-tagged-secondary antibody. Fluorescence captured by confocal laser microscope has been further processed, and the measured intensities were statistically analyzed ( 3 ).

    Article Snippet: The prepared slides were histologically visualized by means of hematoxylin and eosin (H&E) and an inverted light microscope (Axiovert 25, Carl Zeiss, Germany) assembled with a cooled charge-coupled device (CCD) camera (AxioCam HRc).

    Techniques: Injection, Comparison, Staining, Light Microscopy, Incubation, Fluorescence, Microscopy