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optical microscope  (Olympus)


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    Structured Review

    Olympus optical microscope
    Optical Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 3928 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/optical+microscope/CKX53+Cell+Culture+Microscope/pmc13034405-97-11-14
    Average 99 stars, based on 3928 article reviews
    optical microscope - by Bioz Stars, 2026-11
    99/100 stars

    Images

    Related Articles

    Inverted Microscopy:

    Article Title: FOXC2 regulates macrophage polarization and osteosarcoma progression via the CXCL12/CXCR4 signaling axis.
    Article Snippet: Forkhead box protein C2 (FOXC2) is frequently overexpressed in osteosarcoma (OS) and has been implicated in tumor proliferation and metastasis; however, its role in regulating the tumor immune microenvironment remains poorly understood.. In this study, integrative bioinformatics analyses of the TCGA-SARC (The Cancer Genome Atlas sarcoma cohort) dataset were performed to evaluate the clinical significance of FOXC2 in OS.. High FOXC2 expression was significantly associated with poorer overall survival in patients with OS (p < 0.001).

    other:

    Article Title: Elucidation of Selective Apoptosis of Breast Cancer Cells Induced by Panax ginseng –Derived Exosomes via Regulation of Bax/Bcl‐2 Ratio and AMPK‐ α Signaling
    Article Snippet: After PBS washes, Alexa Fluor 594–conjugated secondary antibodies (Thermo Fisher) were added for 1 h at 4.0°C in the dark, followed by nuclear counterstaining with 4 ′ ,6‐diamidino‐2‐phenylindole (DAPI; Thermo Fisher) for 10 min. Fluorescence images were obtained using an inverted microscope (CKX53, Olympus, Shinjuku, Tokyo, Japan) with consistent exposure and gain.

    Article Title: Keap1 Deficiency Promotes Macrophage M2 Polarization and Protects β Cells
    Article Snippet: Images were captured on a fluorescence microscope (CKX53, Olympus Corporation, Tokyo, Japan).

    Cell Culture:

    Article Title: Effect of Dermal Fibroblast‐Conditioned Media on Human Dermal Fibroblasts Treated With Electromagnetic Transduction Therapy
    Article Snippet: For the wound healing assay, HDFs at passages 5 and 25 were seeded into cell culture dishes (μ‐Dish 35 mm‐low; ibidi GmbH, Gräfelfing, Germany) at a density of 1.25 ×10 5 cells/well with cell inserts (Culture‐Insert 2 Well, Cat. #80206; ibidi GmbH) for generating a linear wound and incubated at 37°C in a 5% CO2 incubator for 48 h. Before EMTT, the medium was exchanged with 0%, 30%, and 60% HDFCM, and the cells were treated with 40‐ and 80‐mT EMTT. .. Immediately after EMTT treatment, the cell inserts were removed and cultured for 0, 6, 12, and 24 h. Images of the cells were obtained at each time point under a phase‐contrast light microscope at ×40 magnification (Olympus CKX53; Olympus Life Science, Tokyo, Japan). .. The area of the wound region was measured using ImageJ software (NIH, Bethesda, MD, USA) [ , ].

    Phase Contrast:

    Article Title: Effect of Dermal Fibroblast‐Conditioned Media on Human Dermal Fibroblasts Treated With Electromagnetic Transduction Therapy
    Article Snippet: For the wound healing assay, HDFs at passages 5 and 25 were seeded into cell culture dishes (μ‐Dish 35 mm‐low; ibidi GmbH, Gräfelfing, Germany) at a density of 1.25 ×10 5 cells/well with cell inserts (Culture‐Insert 2 Well, Cat. #80206; ibidi GmbH) for generating a linear wound and incubated at 37°C in a 5% CO2 incubator for 48 h. Before EMTT, the medium was exchanged with 0%, 30%, and 60% HDFCM, and the cells were treated with 40‐ and 80‐mT EMTT. .. Immediately after EMTT treatment, the cell inserts were removed and cultured for 0, 6, 12, and 24 h. Images of the cells were obtained at each time point under a phase‐contrast light microscope at ×40 magnification (Olympus CKX53; Olympus Life Science, Tokyo, Japan). .. The area of the wound region was measured using ImageJ software (NIH, Bethesda, MD, USA) [ , ].

    Light Microscopy:

    Article Title: Effect of Dermal Fibroblast‐Conditioned Media on Human Dermal Fibroblasts Treated With Electromagnetic Transduction Therapy
    Article Snippet: For the wound healing assay, HDFs at passages 5 and 25 were seeded into cell culture dishes (μ‐Dish 35 mm‐low; ibidi GmbH, Gräfelfing, Germany) at a density of 1.25 ×10 5 cells/well with cell inserts (Culture‐Insert 2 Well, Cat. #80206; ibidi GmbH) for generating a linear wound and incubated at 37°C in a 5% CO2 incubator for 48 h. Before EMTT, the medium was exchanged with 0%, 30%, and 60% HDFCM, and the cells were treated with 40‐ and 80‐mT EMTT. .. Immediately after EMTT treatment, the cell inserts were removed and cultured for 0, 6, 12, and 24 h. Images of the cells were obtained at each time point under a phase‐contrast light microscope at ×40 magnification (Olympus CKX53; Olympus Life Science, Tokyo, Japan). .. The area of the wound region was measured using ImageJ software (NIH, Bethesda, MD, USA) [ , ].

    Fluorescence:

    Article Title: The PGC-1α Axis Links Estrogen Receptor-α Signaling to Japanese Encephalitis Virus Replication in Neuronal Cells
    Article Snippet: .. Slides were examined under an upright Olympus Fluorescence microscope (CKX53). ..

    Article Title: Peptide–AuNP–drug conjugate-integrated photocrosslinkable hydrogel with pH/glutathione dual-responsive drug delivery and NIR-triggered heating for combined chemo-photothermal treatment
    Article Snippet: Temperature variations during NIR exposure were monitored using an infrared thermal camera (FOTRIC 220S, FOTRIC, China). .. Calcein-AM/PI fluorescence images were collected with an inverted fluorescence microscope (CKX53, Olympus, Tokyo, Japan). .. The elemental composition of the samples was determined using an inductively coupled plasma instrument (Avio 200, PerkinElmer, USA).

    Article Title: Mature Adipocyte-Derived Extracellular Vesicles Activate Hepatic Stellate Cells and Promote Liver Fibrosis via Inflammation.
    Article Snippet: Background and Aims: Extracellular vesicles (EVs) play a crucial role in intercellular communication, particularly in metabolic regulation and liver disease.. This study aimed to investigate the differential effects of EVs derived from preadipocytes (PA) and mature adipocytes (MA) on hepatic stellate cell (HSC) activation in vitro and their role in promoting liver fibrosis in highfat

    Microscopy:

    Article Title: The PGC-1α Axis Links Estrogen Receptor-α Signaling to Japanese Encephalitis Virus Replication in Neuronal Cells
    Article Snippet: .. Slides were examined under an upright Olympus Fluorescence microscope (CKX53). ..

    Article Title: Peptide–AuNP–drug conjugate-integrated photocrosslinkable hydrogel with pH/glutathione dual-responsive drug delivery and NIR-triggered heating for combined chemo-photothermal treatment
    Article Snippet: Temperature variations during NIR exposure were monitored using an infrared thermal camera (FOTRIC 220S, FOTRIC, China). .. Calcein-AM/PI fluorescence images were collected with an inverted fluorescence microscope (CKX53, Olympus, Tokyo, Japan). .. The elemental composition of the samples was determined using an inductively coupled plasma instrument (Avio 200, PerkinElmer, USA).

    Article Title: Mature Adipocyte-Derived Extracellular Vesicles Activate Hepatic Stellate Cells and Promote Liver Fibrosis via Inflammation.
    Article Snippet: Background and Aims: Extracellular vesicles (EVs) play a crucial role in intercellular communication, particularly in metabolic regulation and liver disease.. This study aimed to investigate the differential effects of EVs derived from preadipocytes (PA) and mature adipocytes (MA) on hepatic stellate cell (HSC) activation in vitro and their role in promoting liver fibrosis in highfat

    Imaging:

    Article Title: Coffee-ring effect enables correlative super-resolution imaging of label-free chromosomes.
    Article Snippet: .. Imaging methods ptical microscopes (Olympus CKX53, Nikon Eclipse LV100ND) were used to c solation. ..



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