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carl zeiss axiovert 135  (Carl Zeiss)


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    Carl Zeiss carl zeiss axiovert 135
    Carl Zeiss Axiovert 135, 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/carl+zeiss+axiovert+135/200m+axiovert+microscope/bio_rxiv__2025__06__23__661024-258-9-9
    Average 90 stars, based on 1 article reviews
    carl zeiss axiovert 135 - by Bioz Stars, 2026-10
    90/100 stars

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    Article Title: Large-scale phenotyping and comparative genomics reveal genetic features of Listeria persistence in epithelial cells
    Article Snippet: Samples were mounted on glass slides and analyzed using Carl Zeiss Axiovert 135.



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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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    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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    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