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axiovert 220 m with a scanning head lsm 5 pa confocal microscope  (Carl Zeiss)


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    Carl Zeiss axiovert 220 m with a scanning head lsm 5 pa confocal microscope
    Axiovert 220 M With A Scanning Head Lsm 5 Pa Confocal Microscope, 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/axiovert+confocal+scanning+microscope/220+axiovert+inverted+microscope/pm40425824-70-20-9
    Average 90 stars, based on 1 article reviews
    axiovert 220 m with a scanning head lsm 5 pa confocal microscope - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Microscopy:

    Article Title: Cryptococcus neoformans glycoantigens are captured by multiple lectin receptors and presented by dendritic cells.
    Article Snippet: .. All samples were imaged using a 60 oil immersion objective on a Zeiss Axiovert Confocal Scanning Microscope. ..

    Article Title: Enhancing glioblastoma cell sensitivity to chemotherapeutics: A strategy involving survivin gene silencing mediated by gemini surfactant-based complexes.
    Article Snippet: http://dx.doi.org/10.1016/j.ejpb.2016.04.014 0939-6411/ 2016 Elsevier B.V. All rights reserved.. ⇑ Corresponding author at: Department of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Calçada Martins de Freitas, 3000-456 Coimbra, Portugal.. E-mail address: asjurado@bioq.uc.pt (A.S. Jurado).

    Article Title: siRNA delivery by a transferrin-associated lipid-based vector: a non-viral strategy to mediate gene silencing.
    Article Snippet: .. All observations were made using a Axiovert confocal scanning microscope (Zeiss, Jena, Germany), under the 60× oil immersion objective. .. Fluorescence-activated cell sorting (FACS) analysis Flow cytometric data were obtained in a Cyan MLE flow cytometer (DaKoCytomation, Copenhagen, Denmark).

    Fluorescence:

    Article Title: Enhancing glioblastoma cell sensitivity to chemotherapeutics: A strategy involving survivin gene silencing mediated by gemini surfactant-based complexes.
    Article Snippet: http://dx.doi.org/10.1016/j.ejpb.2016.04.014 0939-6411/ 2016 Elsevier B.V. All rights reserved.. ⇑ Corresponding author at: Department of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Calçada Martins de Freitas, 3000-456 Coimbra, Portugal.. E-mail address: asjurado@bioq.uc.pt (A.S. Jurado).



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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