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nikon eclipse e800 microscope  (Bergman Labora AB)

 
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    Bergman Labora AB nikon eclipse e800 microscope
    Nikon Eclipse E800 Microscope, supplied by Bergman Labora AB, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/eclipse+e800+light+microscope/nikon+eclipse+e800+microscope/pm34187579-71-14-18
    Average 86 stars, based on 1 article reviews
    nikon eclipse e800 microscope - by Bioz Stars, 2026-11
    86/100 stars

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    Related Articles

    Microscopy:

    Article Title: Age-related changes in brain phospholipids and bioactive lipids in the APP knock-in mouse model of Alzheimer's disease.
    Article Snippet: After washing in 0.01 M phosphate‐buffered saline (PBS), pH 7.4, the immunoreactivity was detected indirectly using secondary antibodies conjugated with Alexa Fluor 488 or 594 for immunofluorescence, or with the Polyvalent HRP/DAB detection kit (Abcam, Cambridge, USA). .. After washing, sections were mounted and examined with a Leica epifluorescence microscope or a Nikon Eclipse E800 microscope (Bergman-Labora, Stockholm, Sweden). ..



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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.
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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