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axio observer d1 inverted fluorescence microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss axio observer d1 inverted fluorescence microscope
    Axio Observer D1 Inverted Fluorescence Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 5062 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/axio+observer+3+inverted+fluorescence+microscope/Inverted+microscope+Axio+Observer+3/pm42909479-65-8-14
    Average 99 stars, based on 5062 article reviews
    axio observer d1 inverted fluorescence microscope - by Bioz Stars, 2026-11
    99/100 stars

    Images

    Related Articles

    Transfection:

    Article Title: YTHDF1 regulates the proliferation and differentiation of keratinocytes via the PI3K/AKT signaling pathway in atopic dermatitis.
    Article Snippet: HaCaT cells were transfected with YTHDF1 overexpression and knockdown lentivirus (Genepharma, Shanghai, China) using an optimal lentivirus concentration of 1 108 TU/ml þ polybrene (MOI 1⁄4 20). .. After 72 h, the survival and transfection efficiency of the cells were observed under an Axio Observer 3 inverted fluorescence microscope (Zeiss, Jena, Germany). ..

    Fluorescence:

    Article Title: YTHDF1 regulates the proliferation and differentiation of keratinocytes via the PI3K/AKT signaling pathway in atopic dermatitis.
    Article Snippet: HaCaT cells were transfected with YTHDF1 overexpression and knockdown lentivirus (Genepharma, Shanghai, China) using an optimal lentivirus concentration of 1 108 TU/ml þ polybrene (MOI 1⁄4 20). .. After 72 h, the survival and transfection efficiency of the cells were observed under an Axio Observer 3 inverted fluorescence microscope (Zeiss, Jena, Germany). ..

    Article Title: Combined Multi-Omics Analysis Reveals the Potential Role of Methionine in Regulating the Proliferation, Differentiation, and Lipid Deposition of Yak Intramuscular Preadipocytes.
    Article Snippet: .. The images were captured using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss, Oberkochen, Germany). .. ImageJ software (version 1.54d, National Institutes of Health, Stapelton, NY, USA) was used to quantify the mean fluorescence intensity from at least six random fields per group.

    Article Title: Combined Multi-Omics Analysis Reveals the Potential Role of Methionine in Regulating the Proliferation, Differentiation, and Lipid Deposition of Yak Intramuscular Preadipocytes
    Article Snippet: .. The images were captured using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss, Oberkochen, Germany). .. ImageJ software (version 1.54d, National Institutes of Health, Stapelton, NY, USA) was used to quantify the mean fluorescence intensity from at least six random fields per group.

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity
    Article Snippet: The nuclei were counterstained with Hoechst 33342 (Thermo Fisher Scientific). .. The Coppersensor-1-labeled cells were imaged using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss, Berlin, Germany), and Coppersonsor-1 fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity
    Article Snippet: Subsequently, the detection reagent was removed, and cells were washed with 1× PBS before counterstaining of nuclei with Hoechst 33342 (Thermo Fisher Scientific) and covered with a cover glass. .. Aggresomes and nuclei were visualized using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss), and aggresome fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Article Title: Microfluidic Perfusable Pathological Vasculature for Atherosclerosis Drug Screening
    Article Snippet: To assess the diffusivity of the perfusable channel, a culture medium containing 25 μg/ml FITC-labeled dextran (Macklin, China) was introduced into the construct. .. The FITC-dextran was allowed to diffuse from the lumen into the GelMA layer for 45 min. Diffusion patterns were monitored using a Zeiss Axio Observer 3 inverted fluorescence microscope (Germany). .. Fluorescence images were captured at 0, 15, 30, and 45 min, and the fluorescence intensity within the microfluidic structure was quantified using ImageJ software.

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity.
    Article Snippet: Subsequently, the detection reagent was removed, and cells were washed with 1× PBS before counterstaining of nuclei with Hoechst 33342 (Thermo Fisher Scientific) and covered with a cover glass. .. Aggresomes and nuclei were visualized using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss), and aggresome fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Microscopy:

    Article Title: YTHDF1 regulates the proliferation and differentiation of keratinocytes via the PI3K/AKT signaling pathway in atopic dermatitis.
    Article Snippet: HaCaT cells were transfected with YTHDF1 overexpression and knockdown lentivirus (Genepharma, Shanghai, China) using an optimal lentivirus concentration of 1 108 TU/ml þ polybrene (MOI 1⁄4 20). .. After 72 h, the survival and transfection efficiency of the cells were observed under an Axio Observer 3 inverted fluorescence microscope (Zeiss, Jena, Germany). ..

    Article Title: Combined Multi-Omics Analysis Reveals the Potential Role of Methionine in Regulating the Proliferation, Differentiation, and Lipid Deposition of Yak Intramuscular Preadipocytes.
    Article Snippet: .. The images were captured using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss, Oberkochen, Germany). .. ImageJ software (version 1.54d, National Institutes of Health, Stapelton, NY, USA) was used to quantify the mean fluorescence intensity from at least six random fields per group.

    Article Title: Combined Multi-Omics Analysis Reveals the Potential Role of Methionine in Regulating the Proliferation, Differentiation, and Lipid Deposition of Yak Intramuscular Preadipocytes
    Article Snippet: .. The images were captured using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss, Oberkochen, Germany). .. ImageJ software (version 1.54d, National Institutes of Health, Stapelton, NY, USA) was used to quantify the mean fluorescence intensity from at least six random fields per group.

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity
    Article Snippet: The nuclei were counterstained with Hoechst 33342 (Thermo Fisher Scientific). .. The Coppersensor-1-labeled cells were imaged using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss, Berlin, Germany), and Coppersonsor-1 fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity
    Article Snippet: Subsequently, the detection reagent was removed, and cells were washed with 1× PBS before counterstaining of nuclei with Hoechst 33342 (Thermo Fisher Scientific) and covered with a cover glass. .. Aggresomes and nuclei were visualized using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss), and aggresome fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Article Title: Microfluidic Perfusable Pathological Vasculature for Atherosclerosis Drug Screening
    Article Snippet: To assess the diffusivity of the perfusable channel, a culture medium containing 25 μg/ml FITC-labeled dextran (Macklin, China) was introduced into the construct. .. The FITC-dextran was allowed to diffuse from the lumen into the GelMA layer for 45 min. Diffusion patterns were monitored using a Zeiss Axio Observer 3 inverted fluorescence microscope (Germany). .. Fluorescence images were captured at 0, 15, 30, and 45 min, and the fluorescence intensity within the microfluidic structure was quantified using ImageJ software.

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity.
    Article Snippet: Subsequently, the detection reagent was removed, and cells were washed with 1× PBS before counterstaining of nuclei with Hoechst 33342 (Thermo Fisher Scientific) and covered with a cover glass. .. Aggresomes and nuclei were visualized using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss), and aggresome fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Software:

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity
    Article Snippet: The nuclei were counterstained with Hoechst 33342 (Thermo Fisher Scientific). .. The Coppersensor-1-labeled cells were imaged using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss, Berlin, Germany), and Coppersonsor-1 fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity
    Article Snippet: Subsequently, the detection reagent was removed, and cells were washed with 1× PBS before counterstaining of nuclei with Hoechst 33342 (Thermo Fisher Scientific) and covered with a cover glass. .. Aggresomes and nuclei were visualized using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss), and aggresome fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Article Title: The Role of Heat Shock Factor 1 in Preserving Proteomic Integrity During Copper-Induced Cellular Toxicity.
    Article Snippet: Subsequently, the detection reagent was removed, and cells were washed with 1× PBS before counterstaining of nuclei with Hoechst 33342 (Thermo Fisher Scientific) and covered with a cover glass. .. Aggresomes and nuclei were visualized using an Axio Observer 3 inverted fluorescence microscope (Carl Zeiss), and aggresome fluorescence intensity was quantified using Image J software (Version 2.3.0) (NIH). ..

    Diffusion-based Assay:

    Article Title: Microfluidic Perfusable Pathological Vasculature for Atherosclerosis Drug Screening
    Article Snippet: To assess the diffusivity of the perfusable channel, a culture medium containing 25 μg/ml FITC-labeled dextran (Macklin, China) was introduced into the construct. .. The FITC-dextran was allowed to diffuse from the lumen into the GelMA layer for 45 min. Diffusion patterns were monitored using a Zeiss Axio Observer 3 inverted fluorescence microscope (Germany). .. Fluorescence images were captured at 0, 15, 30, and 45 min, and the fluorescence intensity within the microfluidic structure was quantified using ImageJ software.

    other:

    Article Title: Microfluidic Perfusable Pathological Vasculature for Atherosclerosis Drug Screening
    Article Snippet: To assess the diffusivity of the perfusable channel, a culture medium containing 25 μg/mL FITC-labeled dextran (Macklin, China) was introduced into the construct.



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