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eclipse e800 light microscope  (Nikon)


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    Structured Review

    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.
    Eclipse E800 Light Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 57094 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+e800+light+microscope/pmc12327690-298-10-9?v=Nikon
    Average 99 stars, based on 57094 article reviews
    eclipse e800 light microscope - by Bioz Stars, 2026-06
    99/100 stars

    Images

    1) Product Images from "Secreted LysM proteins are required for niche competition and full virulence in Pseudomonas savastanoi during host plant infection"

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

    Journal: PLOS Pathogens

    doi: 10.1371/journal.ppat.1013121

    (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.
    Figure Legend 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.

    Techniques Used: Microscopy, Incubation, Light Microscopy, Standard Deviation



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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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    (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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    (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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    (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.
    Light 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+light+microscope/pm39969203-250-5-11?v=Nikon
    Average 90 stars, based on 1 article reviews
    light microscope eclipse e800 - by Bioz Stars, 2026-06
    90/100 stars
      Buy from Supplier

    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