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optical microscope eclipse e800  (Nikon)


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    Structured Review

    Nikon optical microscope eclipse e800
    Optical Microscope Eclipse E800, supplied by Nikon, 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/eclipse+e800+microscope/pmc11974646-63-3-6
    Average 90 stars, based on 1 article reviews
    optical microscope eclipse e800 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title:
    Article Snippet: Visualization of γ-H2AX in Daudi nuclei following AA3 treatment at 60X magnification using Nikon E800 fluorescence microscope.

    Article Title: Bilayer book- like decellularized extracellular matrix scaffold with bioactive coatings for rotator cuff repair
    Article Snippet: Polarized light microscopy (Eclipse E800, Nikon) was used to examine the collagenous organization of tendons near the greater tuberosity in bitter almond red slides.

    Article Title: Nerve root magnetic stimulation regulates the synaptic plasticity of injured spinal cord by ascending sensory pathway
    Article Snippet: Under an optical microscope (Eclipse E800, Nikon, Tokyo, Japan), one field of view centered around the damaged area was selected for each slice, with 12 images per group.

    Article Title: TRESK background potassium channel regulates MrgprA3 + pruriceptor excitability, acute and chronic itch.
    Article Snippet: A subset of peripheral sensory neurons expressing specific Mas-related G-protein–coupled receptors and transient receptor potential channels mediate pruritogen-induced chemical itch.. However, the molecular mechanisms that regulate the excitability of these cells, and consequently itch sensation, are poorly understood.. TWIK-related spinal cord K channel (TRESK) is a background K channel that modulates the restingmembrane potential, action potential firing, and neuronal excitability, and it has been involved in somatosensation and pain transduction.

    Article Title: POMC neurons control fertility through differential signaling of MC4R in kisspeptin neurons
    Article Snippet: Photomicrographs of labeling were initially acquired using a Nikon E800 fluorescent microscope (Eclipse E800; Nikon Instruments, Melville, NY) equipped with a fiber illuminator (Intensilight C-HGFI; Nikon Instruments) and a high-definition digital microscope camera head (DS-Fi1; Nikon Instruments) interfaced with a PC-based camera controller (DS-U3; Nikon Instruments).

    Microscopy:

    Article Title: Supporting Information
    Article Snippet: A syringe pump (Lagato210P, KD Scientific, Holliston, MA) was used to withdraw liquid from a reservoir of fluorescent particle-containing DI water (Fluoro-Max Green and Red Dry Fluorescent Particles, Thermo Fisher, Waltham, MA) into the construct (Figure S9c), using the same pulse flow pattern employed for miniJoint cultures. .. Three videos of the fluid flow were recorded using a Nikon Eclipse E800 upright microscope (Nikon, Melville, S-5 NY) during the fast flow stage. ..

    Article Title:
    Article Snippet: Axio Lab A1 microscope, Canon EOS 1000D camera with AxioVision software (Carl Zeiss, AxioVision Rel. .. 4.8 Ink.), Nikon ECLIPSE E800 epifluorescence microscope, and QImaging RETGA EXi camera with QCapture software (QImaging v7.0) were used for imaging. ..

    Staining:

    Article Title: Supporting Information
    Article Snippet: .. Images of picrosirius red staining were taken using a polarized light microscope (Eclipse E800, Nikon). ..

    Light Microscopy:

    Article Title: Supporting Information
    Article Snippet: .. Images of picrosirius red staining were taken using a polarized light microscope (Eclipse E800, Nikon). ..

    Imaging:

    Article Title:
    Article Snippet: Axio Lab A1 microscope, Canon EOS 1000D camera with AxioVision software (Carl Zeiss, AxioVision Rel. .. 4.8 Ink.), Nikon ECLIPSE E800 epifluorescence microscope, and QImaging RETGA EXi camera with QCapture software (QImaging v7.0) were used for imaging. ..



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    Nikon eclipse e800 light microscope
    (A) Twitching motility on 1%-agar KB medium overlaid on slides by the wild-type strain Psv NCPPB 3335 (Psv) and the Δ lysM mutants. Microscopy images were taken after 24h of incubation at 25°C with Nikon Eclipse <t>E800</t> light <t>microscope</t> (20x). The experiment was repeated three times with two repetitions per trial, and a representative image is shown per strain. (B-C) Swimming motility on 0.3%-agar KB medium. (B) Representative images of swimming halos formed by the wild-type strain Psv and the Δ lysM mutants after three days of incubation at 25°C. (C) Swimming halos are represented as the covered area (cm 2 ). Data are presented as means and standard deviation (SD) from three independent experiments, with at least four replicas per assay. Asterisks indicate statistically significant differences (ANOVA test; p < 0.0001), and “ns” indicates no significant differences between samples.
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    Nikon eclipse e800 upright microscope
    (A) Twitching motility on 1%-agar KB medium overlaid on slides by the wild-type strain Psv NCPPB 3335 (Psv) and the Δ lysM mutants. Microscopy images were taken after 24h of incubation at 25°C with Nikon Eclipse <t>E800</t> light <t>microscope</t> (20x). The experiment was repeated three times with two repetitions per trial, and a representative image is shown per strain. (B-C) Swimming motility on 0.3%-agar KB medium. (B) Representative images of swimming halos formed by the wild-type strain Psv and the Δ lysM mutants after three days of incubation at 25°C. (C) Swimming halos are represented as the covered area (cm 2 ). Data are presented as means and standard deviation (SD) from three independent experiments, with at least four replicas per assay. Asterisks indicate statistically significant differences (ANOVA test; p < 0.0001), and “ns” indicates no significant differences between samples.
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    Image Search Results


    (A) Twitching motility on 1%-agar KB medium overlaid on slides by the wild-type strain Psv NCPPB 3335 (Psv) and the Δ lysM mutants. Microscopy images were taken after 24h of incubation at 25°C with Nikon Eclipse E800 light microscope (20x). The experiment was repeated three times with two repetitions per trial, and a representative image is shown per strain. (B-C) Swimming motility on 0.3%-agar KB medium. (B) Representative images of swimming halos formed by the wild-type strain Psv and the Δ lysM mutants after three days of incubation at 25°C. (C) Swimming halos are represented as the covered area (cm 2 ). Data are presented as means and standard deviation (SD) from three independent experiments, with at least four replicas per assay. Asterisks indicate statistically significant differences (ANOVA test; p < 0.0001), and “ns” indicates no significant differences between samples.

    Journal: PLOS Pathogens

    Article Title: Secreted LysM proteins are required for niche competition and full virulence in Pseudomonas savastanoi during host plant infection

    doi: 10.1371/journal.ppat.1013121

    Figure Lengend Snippet: (A) Twitching motility on 1%-agar KB medium overlaid on slides by the wild-type strain Psv NCPPB 3335 (Psv) and the Δ lysM mutants. Microscopy images were taken after 24h of incubation at 25°C with Nikon Eclipse E800 light microscope (20x). The experiment was repeated three times with two repetitions per trial, and a representative image is shown per strain. (B-C) Swimming motility on 0.3%-agar KB medium. (B) Representative images of swimming halos formed by the wild-type strain Psv and the Δ lysM mutants after three days of incubation at 25°C. (C) Swimming halos are represented as the covered area (cm 2 ). Data are presented as means and standard deviation (SD) from three independent experiments, with at least four replicas per assay. Asterisks indicate statistically significant differences (ANOVA test; p < 0.0001), and “ns” indicates no significant differences between samples.

    Article Snippet: After incubation, the twitching areas were examined using a Nikon Eclipse E800 light microscope with a 20x objective lens.

    Techniques: Microscopy, Incubation, Light Microscopy, Standard Deviation