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cell morphologic changes  (Olympus)


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    Structured Review

    Olympus cell morphologic changes
    Cell Morphologic Changes, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 3900 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cell+morphologic+changes/CKX53+Cell+Culture+Microscope/pm38867145-89-0-11
    Average 99 stars, based on 3900 article reviews
    cell morphologic changes - by Bioz Stars, 2026-10
    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: Ent-7β-hydroxy-15-oxokaur-16-en-18-yl acetate suppresses RANKL-induced and LPS-enhanced osteoclastogenesis through NF-κB/MAPK signaling with involvement of the ACE-AT1R axis.
    Article Snippet: TRAP-positive multinucleated cells containing three or more nuclei were counted under the microscope (CKX 53, Olympus, Tokyo, Japan).

    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) [ , ].

    Microscopy:

    Article Title: Applicability of the defined solid angle method to the activity measurement of α-emitters for targeted radionuclide therapy.
    Article Snippet: We investigated the applicability of the defined solid angle (DSA) approach as a basis for activity measurement of therapeutic α-emitters, focusing on 223Ra and 225Ac.. Diaphragms with different aperture diameters were fabricated using a 3D printer and employed to delimit the sensitive area.. The heterogeneity of the source activity distribution was evaluated using an imaging plate, and Monte Carlo simulations were employed to calculate the effective solid angle, explicitly accounting for the non-uniform distribution of activity on the source surface.

    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

    Fluorescence:

    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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