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n structured illumination superresolution microscope  (Nikon)


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    Nikon n structured illumination superresolution microscope
    N Structured Illumination Superresolution Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59743 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/n+structured+illumination+superresolution+microscope/Objectives/10__1091_slash_mbc__e23___12___0515-123-22-21
    Average 99 stars, based on 59743 article reviews
    n structured illumination superresolution microscope - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Imaging:

    Article Title: <i>Giardia's</i> domed ventral disc architecture is essential for attachment and contributes to epithelial barrier disruption
    Article Snippet: Giardia lamblia is a widespread anaerobic protistan parasite causing significant diarrheal disease worldwide.. Giardia trophozoites attach extracellularly to the host gastrointestinal epithelium using a unique microtubule organelle, the ventral disc.. The complex, dome-shaped disc is composed of microribbon-crossbridge (MR-CB) protein complexes scaffolded onto a spiral microtubule array.

    Microscopy:

    Article Title: <i>Giardia's</i> domed ventral disc architecture is essential for attachment and contributes to epithelial barrier disruption
    Article Snippet: Giardia lamblia is a widespread anaerobic protistan parasite causing significant diarrheal disease worldwide.. Giardia trophozoites attach extracellularly to the host gastrointestinal epithelium using a unique microtubule organelle, the ventral disc.. The complex, dome-shaped disc is composed of microribbon-crossbridge (MR-CB) protein complexes scaffolded onto a spiral microtubule array.



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    SIM enables precise imaging of AβOs bound to spines. SIM was used to determine the binding of AβOs to primary hippocampal neurons, using the N-SIM <t>superresolution</t> <t>microscope</t> with a lateral resolution at 100× of ∼100 nm, compared with the more typical 400 nm of most microscopes. Primary hippocampal cells, cultured for 19 d, were treated with 100 nM AβOs for 1 h and immunolabeled with anti-TuJ (green) and NU4 (magenta).
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    Image Search Results


    SIM enables precise imaging of AβOs bound to spines. SIM was used to determine the binding of AβOs to primary hippocampal neurons, using the N-SIM superresolution microscope with a lateral resolution at 100× of ∼100 nm, compared with the more typical 400 nm of most microscopes. Primary hippocampal cells, cultured for 19 d, were treated with 100 nM AβOs for 1 h and immunolabeled with anti-TuJ (green) and NU4 (magenta).

    Journal: Molecular Biology of the Cell

    Article Title: Neuroprotective astrocyte-derived insulin/insulin-like growth factor 1 stimulates endocytic processing and extracellular release of neuron-bound Aβ oligomers

    doi: 10.1091/mbc.E17-06-0416

    Figure Lengend Snippet: SIM enables precise imaging of AβOs bound to spines. SIM was used to determine the binding of AβOs to primary hippocampal neurons, using the N-SIM superresolution microscope with a lateral resolution at 100× of ∼100 nm, compared with the more typical 400 nm of most microscopes. Primary hippocampal cells, cultured for 19 d, were treated with 100 nM AβOs for 1 h and immunolabeled with anti-TuJ (green) and NU4 (magenta).

    Article Snippet: N-SIM images were captured on a Nikon N-SIM Structured Illumination superresolution microscope.

    Techniques: Imaging, Binding Assay, Microscopy, Cell Culture, Immunolabeling