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axio observer inverted microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss axio observer inverted microscope
    Axio Observer Inverted Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 1984 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/inverted+microscope/Primovert+Compact+Inverted+Microscope/pm42811434-52-7-6
    Average 99 stars, based on 1984 article reviews
    axio observer inverted microscope - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    other:

    Article Title: Baihe Zhimu Decoction ameliorates anxious depression via PI3K / AKT / mTOR pathway‐mediated neuroprotection and inhibition of hippocampal neuronal apoptosis
    Article Snippet: Cellular morphology was observed under an inverted microscope (Zeiss, Germany), and neuronal purity was confirmed by NSE immunofluorescence.

    Article Title: Hypothalamus Participates in Peripheral Sympathetic Hyperactivity After Acute Brain Injury by Regulating Trhr M 6 A Modification
    Article Snippet: After axonal baseline Ca 2+ fluorescence intensity was recorded for 1 min, 20 μM Ca 2+ or 5 μM TRH was added to the culture, and constant images were recorded for 2 min with an inverted microscope (Zeiss, Germany).

    Article Title: Innovative antifungal therapy using Brij®-capped flexosomes loaded with Aripiprazole for Candida albicans associated vaginal infection.
    Article Snippet: Aim and background: This study aimed to investigate Aripiprazole (ARP) as a repurposed antifungal drug within Brij-Capped flexosomes (O-FLs) mucoadhesive gel against vaginal candidiasis.. Methods: ARP-FLs prepared by thin-film hydration was optimized using a 23 factorial design to evaluate the effects of Edge Activator (EA) (X1), phospholipid amount (X2) (mg), and cationic surfactants (X3) on entrapment efficiency (EE%; Y1), particle size (PS; Y2), polydispersity index (PDI; Y3), and zeta potential (ZP; Y4).. The best ARP-FLs were identified for optimization using Design-Expert software.

    Spheroids:

    Article Title: Engineering a Functional Angiogenesis-Enabled and Ovarian Cell-Specific Tumor Microenvironment Chip
    Article Snippet: .. Spheroids and devices were imaged using a Zeiss Axio Observer Z1 inverted microscope (Colibri 7 LED, filter set 115). ..

    Inverted Microscopy:

    Article Title: Engineering a Functional Angiogenesis-Enabled and Ovarian Cell-Specific Tumor Microenvironment Chip
    Article Snippet: .. Spheroids and devices were imaged using a Zeiss Axio Observer Z1 inverted microscope (Colibri 7 LED, filter set 115). ..

    Article Title: Pre-splicing factors associate with UpA-rich RNA and limit flavivirus replication.
    Article Snippet: .. Cells were visualized using a Zeiss Axio Observer Z1 inverted microscope at 40x magnification using an oil-immersion objective. ..

    Article Title: Inhibition of Calcium-Sensing Receptor Suppresses Malignant Behaviours of Human Hepatocellular Carcinoma.
    Article Snippet: .. Fluorescence imaging was conducted using a Zeiss Axio Observer inverted microscope (Oberkochen, Germany). ..

    Article Title: Microstructure–property relationships in alpha olefin sulfonate/cocamidopropyl betaine systems: Effects of cocamide monoethanolamine and botanical oil
    Article Snippet: Surfactant-based formulations used in personal care applications derive their performance from a complex interplay between micellar organization, bulk rheology, and interfacial properties.. Although co-surfactants and hydrophobic additives are widely employed to tailor formulation performance on substrates like hair, the relationships linking micellar structure to emulsion and spreading behavior remain poorly understood.. Here, a bottom-up approach was adopted to investigate how cocamide monoethanolamine (CMEA) and a botanical oil (BO) influence the structure–property relationships of alpha olefin sulfonate (AOS)/cocamidopropyl betaine (CapB) formulations.

    Brightfield:

    Article Title: Tomatidine Exposure During Early Myogenesis Promotes Hypertrophy of C2C12 Muscle Cells Through Increased Nuclei Accretion
    Article Snippet: .. Brightfield images were captured daily at 10× magnification using a Zeiss Primovert Microscope with a Zeiss AxioCam ERC 5 s Rev 2.0 camera (Carl Zeiss AG, Germany), to visualize daily morphological changes (Figure , Supplemental Material). ..

    Microscopy:

    Article Title: Tomatidine Exposure During Early Myogenesis Promotes Hypertrophy of C2C12 Muscle Cells Through Increased Nuclei Accretion
    Article Snippet: .. Brightfield images were captured daily at 10× magnification using a Zeiss Primovert Microscope with a Zeiss AxioCam ERC 5 s Rev 2.0 camera (Carl Zeiss AG, Germany), to visualize daily morphological changes (Figure , Supplemental Material). ..

    Article Title: Microstructure–property relationships in alpha olefin sulfonate/cocamidopropyl betaine systems: Effects of cocamide monoethanolamine and botanical oil
    Article Snippet: Surfactant-based formulations used in personal care applications derive their performance from a complex interplay between micellar organization, bulk rheology, and interfacial properties.. Although co-surfactants and hydrophobic additives are widely employed to tailor formulation performance on substrates like hair, the relationships linking micellar structure to emulsion and spreading behavior remain poorly understood.. Here, a bottom-up approach was adopted to investigate how cocamide monoethanolamine (CMEA) and a botanical oil (BO) influence the structure–property relationships of alpha olefin sulfonate (AOS)/cocamidopropyl betaine (CapB) formulations.

    Fluorescence:

    Article Title: Inhibition of Calcium-Sensing Receptor Suppresses Malignant Behaviours of Human Hepatocellular Carcinoma.
    Article Snippet: .. Fluorescence imaging was conducted using a Zeiss Axio Observer inverted microscope (Oberkochen, Germany). ..

    Imaging:

    Article Title: Inhibition of Calcium-Sensing Receptor Suppresses Malignant Behaviours of Human Hepatocellular Carcinoma.
    Article Snippet: .. Fluorescence imaging was conducted using a Zeiss Axio Observer inverted microscope (Oberkochen, Germany). ..

    Confocal:

    Article Title: Microstructure–property relationships in alpha olefin sulfonate/cocamidopropyl betaine systems: Effects of cocamide monoethanolamine and botanical oil
    Article Snippet: Surfactant-based formulations used in personal care applications derive their performance from a complex interplay between micellar organization, bulk rheology, and interfacial properties.. Although co-surfactants and hydrophobic additives are widely employed to tailor formulation performance on substrates like hair, the relationships linking micellar structure to emulsion and spreading behavior remain poorly understood.. Here, a bottom-up approach was adopted to investigate how cocamide monoethanolamine (CMEA) and a botanical oil (BO) influence the structure–property relationships of alpha olefin sulfonate (AOS)/cocamidopropyl betaine (CapB) formulations.



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    The two pediatric medulloblastoma cell lines ONS76 (p53 wild-type) and UW228-3 (p53-mut.) were exposed to 20 Gy γIR. After the indicated time periods, cells were stained for senescence-associated beta-galactosidase activity (manifested in blue) and documented microscopically in phase contrast ( A ) and brightfield ( B ) using a Zeiss <t>Axio</t> <t>Vert.A1</t> microscope. With increasing incubation times after irradiation, ONS76 display a strong blue staining and morphological changes, such as an increase in cell and nucleus size, reminiscing of cellular senescence, whereas UW228-3 cells detach from the bottom and die. All pictures were taken with the same 10× objective and the included 100 µm scale bar is representative for all micrographs. The pictures chosen are representative for at least three independent biological experiments. Please note that detached and dead cells are aspirated during the SA-beta-Galactosidase staining procedure and are therefore not present anymore, in contrast to Supplementary Fig. , in which the cells were photographed under culturing conditions.
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    The two pediatric medulloblastoma cell lines ONS76 (p53 wild-type) and UW228-3 (p53-mut.) were exposed to 20 Gy γIR. After the indicated time periods, cells were stained for senescence-associated beta-galactosidase activity (manifested in blue) and documented microscopically in phase contrast ( A ) and brightfield ( B ) using a Zeiss <t>Axio</t> <t>Vert.A1</t> microscope. With increasing incubation times after irradiation, ONS76 display a strong blue staining and morphological changes, such as an increase in cell and nucleus size, reminiscing of cellular senescence, whereas UW228-3 cells detach from the bottom and die. All pictures were taken with the same 10× objective and the included 100 µm scale bar is representative for all micrographs. The pictures chosen are representative for at least three independent biological experiments. Please note that detached and dead cells are aspirated during the SA-beta-Galactosidase staining procedure and are therefore not present anymore, in contrast to Supplementary Fig. , in which the cells were photographed under culturing conditions.
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    The two pediatric medulloblastoma cell lines ONS76 (p53 wild-type) and UW228-3 (p53-mut.) were exposed to 20 Gy γIR. After the indicated time periods, cells were stained for senescence-associated beta-galactosidase activity (manifested in blue) and documented microscopically in phase contrast ( A ) and brightfield ( B ) using a Zeiss <t>Axio</t> <t>Vert.A1</t> microscope. With increasing incubation times after irradiation, ONS76 display a strong blue staining and morphological changes, such as an increase in cell and nucleus size, reminiscing of cellular senescence, whereas UW228-3 cells detach from the bottom and die. All pictures were taken with the same 10× objective and the included 100 µm scale bar is representative for all micrographs. The pictures chosen are representative for at least three independent biological experiments. Please note that detached and dead cells are aspirated during the SA-beta-Galactosidase staining procedure and are therefore not present anymore, in contrast to Supplementary Fig. , in which the cells were photographed under culturing conditions.
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    The two pediatric medulloblastoma cell lines ONS76 (p53 wild-type) and UW228-3 (p53-mut.) were exposed to 20 Gy γIR. After the indicated time periods, cells were stained for senescence-associated beta-galactosidase activity (manifested in blue) and documented microscopically in phase contrast ( A ) and brightfield ( B ) using a Zeiss <t>Axio</t> <t>Vert.A1</t> microscope. With increasing incubation times after irradiation, ONS76 display a strong blue staining and morphological changes, such as an increase in cell and nucleus size, reminiscing of cellular senescence, whereas UW228-3 cells detach from the bottom and die. All pictures were taken with the same 10× objective and the included 100 µm scale bar is representative for all micrographs. The pictures chosen are representative for at least three independent biological experiments. Please note that detached and dead cells are aspirated during the SA-beta-Galactosidase staining procedure and are therefore not present anymore, in contrast to Supplementary Fig. , in which the cells were photographed under culturing conditions.
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    Image Search Results


    The two pediatric medulloblastoma cell lines ONS76 (p53 wild-type) and UW228-3 (p53-mut.) were exposed to 20 Gy γIR. After the indicated time periods, cells were stained for senescence-associated beta-galactosidase activity (manifested in blue) and documented microscopically in phase contrast ( A ) and brightfield ( B ) using a Zeiss Axio Vert.A1 microscope. With increasing incubation times after irradiation, ONS76 display a strong blue staining and morphological changes, such as an increase in cell and nucleus size, reminiscing of cellular senescence, whereas UW228-3 cells detach from the bottom and die. All pictures were taken with the same 10× objective and the included 100 µm scale bar is representative for all micrographs. The pictures chosen are representative for at least three independent biological experiments. Please note that detached and dead cells are aspirated during the SA-beta-Galactosidase staining procedure and are therefore not present anymore, in contrast to Supplementary Fig. , in which the cells were photographed under culturing conditions.

    Journal: Cell Death Discovery

    Article Title: p53 wild-type/low c-Myc-expressing ONS76 pediatric medulloblastoma cells become senescent after gamma-irradiation and can be eliminated by senolytic substances

    doi: 10.1038/s41420-026-03404-4

    Figure Lengend Snippet: The two pediatric medulloblastoma cell lines ONS76 (p53 wild-type) and UW228-3 (p53-mut.) were exposed to 20 Gy γIR. After the indicated time periods, cells were stained for senescence-associated beta-galactosidase activity (manifested in blue) and documented microscopically in phase contrast ( A ) and brightfield ( B ) using a Zeiss Axio Vert.A1 microscope. With increasing incubation times after irradiation, ONS76 display a strong blue staining and morphological changes, such as an increase in cell and nucleus size, reminiscing of cellular senescence, whereas UW228-3 cells detach from the bottom and die. All pictures were taken with the same 10× objective and the included 100 µm scale bar is representative for all micrographs. The pictures chosen are representative for at least three independent biological experiments. Please note that detached and dead cells are aspirated during the SA-beta-Galactosidase staining procedure and are therefore not present anymore, in contrast to Supplementary Fig. , in which the cells were photographed under culturing conditions.

    Article Snippet: Pictures were taken with 10× or 20× magnification as indicated using the Zeiss Axio Vert.A1 microscope and the associated AxioVision Software (Carl Zeiss MicroImaging GmbH, Göttingen, Germany).

    Techniques: Staining, Activity Assay, Phase Contrast, Brightfield, Microscopy, Incubation, Irradiation