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confocal laser scanning microscopy (nikon eclipse ti-e inverted microscope system)  (Nikon)


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    Nikon confocal laser scanning microscopy (nikon eclipse ti-e inverted microscope system)
    Confocal Laser Scanning Microscopy (Nikon Eclipse Ti E Inverted Microscope System), 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/laser+scanning+confocal+microscopy+nikon+inverted+microscope+eclipse+ti-e/pm40369521-95-4-9
    Average 90 stars, based on 1 article reviews
    confocal laser scanning microscopy (nikon eclipse ti-e inverted microscope system) - by Bioz Stars, 2026-09
    90/100 stars

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    Confocal Laser Scanning Microscopy:

    Article Title: Translational Diffusion Dynamics in Divalent Metal-Phosphonate Monolayers.
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    Article Title: The Interplay between S-Glutathionylation and Phosphorylation of Cardiac Troponin I and Myosin Binding Protein C in End-Stage Human Failing Hearts
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    Inverted Microscopy:

    Article Title: Translational Diffusion Dynamics in Divalent Metal-Phosphonate Monolayers.
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    Article Title: The Interplay between S-Glutathionylation and Phosphorylation of Cardiac Troponin I and Myosin Binding Protein C in End-Stage Human Failing Hearts
    Article Snippet: .. We used imaging confocal laser scanning microscopy (Nikon Eclipse Ti-E Inverted Microscope System; Nikon Instruments, Nikon Corp, Shinagawa, Tokyo, Japan). ..

    Article Title: In-Depth Characterization of a Re-Engineered Cholera Toxin Manufacturing Process Using Growth-Decoupled Production in Escherichia coli .
    Article Snippet: .. Samples were imaged through a laser scanning confocal microscope system (Nikon Eclipse Ti-E inverted microscope equipped with Nikon A1R confocal laser scanning system, 60× oil immersion objective, numerical aperture (NA) of 1.49, with four lasers: 405 nm, 488 nm, 561 nm, and 640 nm). .. The images were further analyzed using NIS-Element Confocal 4.20 from Nikon and ImageJ 1.52a from Laboratory for Optical and Computational Instrumentation.

    Imaging:

    Article Title: The Interplay between S-Glutathionylation and Phosphorylation of Cardiac Troponin I and Myosin Binding Protein C in End-Stage Human Failing Hearts
    Article Snippet: .. We used imaging confocal laser scanning microscopy (Nikon Eclipse Ti-E Inverted Microscope System; Nikon Instruments, Nikon Corp, Shinagawa, Tokyo, Japan). ..

    Microscopy:

    Article Title: In-Depth Characterization of a Re-Engineered Cholera Toxin Manufacturing Process Using Growth-Decoupled Production in Escherichia coli .
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    <t>cLSM</t> images of control and DSS rat cardiomyocytes before and after sGC activator treatment demonstrating sGC translocation to the intercalated disc (A–D) . Representative immunofluorescence images of cardiomyocytes stained for cardiac sGC (red) and counterstained for α-actinin (green). (E–H) Immunofluorescence images of cardiomyocytes stained for connexin 43 (red) and counterstained for α-actinin (green). (I–L) Representative immunofluorecence images of cardiomyocytes stained for connexin 43 (green) and sGC (red).
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    Nikon confocal laser scanning microscopy nikon eclipse ti-e inverted microscope system
    <t>cLSM</t> images of control and DSS rat cardiomyocytes before and after sGC activator treatment demonstrating sGC translocation to the intercalated disc (A–D) . Representative immunofluorescence images of cardiomyocytes stained for cardiac sGC (red) and counterstained for α-actinin (green). (E–H) Immunofluorescence images of cardiomyocytes stained for connexin 43 (red) and counterstained for α-actinin (green). (I–L) Representative immunofluorecence images of cardiomyocytes stained for connexin 43 (green) and sGC (red).
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    Image Search Results


    cLSM images of control and DSS rat cardiomyocytes before and after sGC activator treatment demonstrating sGC translocation to the intercalated disc (A–D) . Representative immunofluorescence images of cardiomyocytes stained for cardiac sGC (red) and counterstained for α-actinin (green). (E–H) Immunofluorescence images of cardiomyocytes stained for connexin 43 (red) and counterstained for α-actinin (green). (I–L) Representative immunofluorecence images of cardiomyocytes stained for connexin 43 (green) and sGC (red).

    Journal: Frontiers in Physiology

    Article Title: Enhanced Cardiomyocyte Function in Hypertensive Rats With Diastolic Dysfunction and Human Heart Failure Patients After Acute Treatment With Soluble Guanylyl Cyclase (sGC) Activator

    doi: 10.3389/fphys.2020.00345

    Figure Lengend Snippet: cLSM images of control and DSS rat cardiomyocytes before and after sGC activator treatment demonstrating sGC translocation to the intercalated disc (A–D) . Representative immunofluorescence images of cardiomyocytes stained for cardiac sGC (red) and counterstained for α-actinin (green). (E–H) Immunofluorescence images of cardiomyocytes stained for connexin 43 (red) and counterstained for α-actinin (green). (I–L) Representative immunofluorecence images of cardiomyocytes stained for connexin 43 (green) and sGC (red).

    Article Snippet: Immuno-stained samples were analyzed by confocal laser scanning microscopy (cLSM) (Nikon Eclipse Ti-E Inverted Microscope System; Nikon Instruments, Nikon Corp, Shinagawa, Tokyo, Japan).

    Techniques: Control, Translocation Assay, Immunofluorescence, Staining