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scanning confocal microscope carl zeiss axiovert 135 m-lsm microsystem  (Carl Zeiss)


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    Carl Zeiss scanning confocal microscope carl zeiss axiovert 135 m-lsm microsystem
    Immunostaining of ADAM17 in C2C12 myotubes. Analysis by immunofluorescence (a) control and (b) myotubes stimulated by 2 h with L-arginine 5 mM. Cells were fixed and incubated with anti-ADAM17 antibody (1:100) and then with secondary antibody Alexa Fluor 546 donkey anti-rabbit IgG (H + L) (1:500). Images were obtained by a confocal <t>microscope</t> ( n = 3). Scale bar = 10 μm.
    Scanning Confocal Microscope Carl Zeiss Axiovert 135 M Lsm Microsystem, supplied by Carl Zeiss, 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/microscope+zeiss+axiovert+135+m/pmc11991828-92-6-9?v=Carl+Zeiss
    Average 90 stars, based on 1 article reviews
    scanning confocal microscope carl zeiss axiovert 135 m-lsm microsystem - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "L-Arginine Activates the Neuregulin-1/ErbB Receptor Signaling Pathway and Increases Utrophin mRNA Levels in C2C12 Cells"

    Article Title: L-Arginine Activates the Neuregulin-1/ErbB Receptor Signaling Pathway and Increases Utrophin mRNA Levels in C2C12 Cells

    Journal: Biochemistry Research International

    doi: 10.1155/bri/2171745

    Immunostaining of ADAM17 in C2C12 myotubes. Analysis by immunofluorescence (a) control and (b) myotubes stimulated by 2 h with L-arginine 5 mM. Cells were fixed and incubated with anti-ADAM17 antibody (1:100) and then with secondary antibody Alexa Fluor 546 donkey anti-rabbit IgG (H + L) (1:500). Images were obtained by a confocal microscope ( n = 3). Scale bar = 10 μm.
    Figure Legend Snippet: Immunostaining of ADAM17 in C2C12 myotubes. Analysis by immunofluorescence (a) control and (b) myotubes stimulated by 2 h with L-arginine 5 mM. Cells were fixed and incubated with anti-ADAM17 antibody (1:100) and then with secondary antibody Alexa Fluor 546 donkey anti-rabbit IgG (H + L) (1:500). Images were obtained by a confocal microscope ( n = 3). Scale bar = 10 μm.

    Techniques Used: Immunostaining, Immunofluorescence, Control, Incubation, Microscopy



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    Immunostaining of ADAM17 in C2C12 myotubes. Analysis by immunofluorescence (a) control and (b) myotubes stimulated by 2 h with L-arginine 5 mM. Cells were fixed and incubated with anti-ADAM17 antibody (1:100) and then with secondary antibody Alexa Fluor 546 donkey anti-rabbit IgG (H + L) (1:500). Images were obtained by a confocal <t>microscope</t> ( n = 3). Scale bar = 10 μm.
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    Image Search Results


    Immunostaining of ADAM17 in C2C12 myotubes. Analysis by immunofluorescence (a) control and (b) myotubes stimulated by 2 h with L-arginine 5 mM. Cells were fixed and incubated with anti-ADAM17 antibody (1:100) and then with secondary antibody Alexa Fluor 546 donkey anti-rabbit IgG (H + L) (1:500). Images were obtained by a confocal microscope ( n = 3). Scale bar = 10 μm.

    Journal: Biochemistry Research International

    Article Title: L-Arginine Activates the Neuregulin-1/ErbB Receptor Signaling Pathway and Increases Utrophin mRNA Levels in C2C12 Cells

    doi: 10.1155/bri/2171745

    Figure Lengend Snippet: Immunostaining of ADAM17 in C2C12 myotubes. Analysis by immunofluorescence (a) control and (b) myotubes stimulated by 2 h with L-arginine 5 mM. Cells were fixed and incubated with anti-ADAM17 antibody (1:100) and then with secondary antibody Alexa Fluor 546 donkey anti-rabbit IgG (H + L) (1:500). Images were obtained by a confocal microscope ( n = 3). Scale bar = 10 μm.

    Article Snippet: The samples were evaluated in a scanning confocal microscope (Carl Zeiss Axiovert 135 m-LSM Microsystem).

    Techniques: Immunostaining, Immunofluorescence, Control, Incubation, Microscopy