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human skin primary fibroblast cells  (ATCC)


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    ATCC human skin primary fibroblast cells
    Confocal microscopy images of <t>WS1</t> <t>fibroblast</t> cells. Bright-field image ( A ) and confocal fluorescence image ( B ) of WS1 cells incubated with IRPhen (10 µM) for 30 min. Bright-field image ( C ) and confocal fluorescence image ( D ) of cells pretreated with Cu 2+ (10 µM) for 8 h, followed by incubation with IRPhen (10 µM) for 30 min; ( E ) Quantitative bar graph showing the corresponding fluorescence intensities of panels ( B , D ). Excitation was at 633 nm, and emission was collected from 650–850 nm. Scale bar, 10 µm.
    Human Skin Primary Fibroblast Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 391 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human skin primary fibroblast cells/product/ATCC
    Average 96 stars, based on 391 article reviews
    human skin primary fibroblast cells - by Bioz Stars, 2026-03
    96/100 stars

    Images

    1) Product Images from "A Heptamethine Cyanine-Based Near-Infrared Optical Sensor for Copper(II) Detection in Aqueous Solutions and Living Cells"

    Article Title: A Heptamethine Cyanine-Based Near-Infrared Optical Sensor for Copper(II) Detection in Aqueous Solutions and Living Cells

    Journal: Sensors (Basel, Switzerland)

    doi: 10.3390/s26010130

    Confocal microscopy images of WS1 fibroblast cells. Bright-field image ( A ) and confocal fluorescence image ( B ) of WS1 cells incubated with IRPhen (10 µM) for 30 min. Bright-field image ( C ) and confocal fluorescence image ( D ) of cells pretreated with Cu 2+ (10 µM) for 8 h, followed by incubation with IRPhen (10 µM) for 30 min; ( E ) Quantitative bar graph showing the corresponding fluorescence intensities of panels ( B , D ). Excitation was at 633 nm, and emission was collected from 650–850 nm. Scale bar, 10 µm.
    Figure Legend Snippet: Confocal microscopy images of WS1 fibroblast cells. Bright-field image ( A ) and confocal fluorescence image ( B ) of WS1 cells incubated with IRPhen (10 µM) for 30 min. Bright-field image ( C ) and confocal fluorescence image ( D ) of cells pretreated with Cu 2+ (10 µM) for 8 h, followed by incubation with IRPhen (10 µM) for 30 min; ( E ) Quantitative bar graph showing the corresponding fluorescence intensities of panels ( B , D ). Excitation was at 633 nm, and emission was collected from 650–850 nm. Scale bar, 10 µm.

    Techniques Used: Confocal Microscopy, Fluorescence, Incubation



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    Image Search Results


    Confocal microscopy images of WS1 fibroblast cells. Bright-field image ( A ) and confocal fluorescence image ( B ) of WS1 cells incubated with IRPhen (10 µM) for 30 min. Bright-field image ( C ) and confocal fluorescence image ( D ) of cells pretreated with Cu 2+ (10 µM) for 8 h, followed by incubation with IRPhen (10 µM) for 30 min; ( E ) Quantitative bar graph showing the corresponding fluorescence intensities of panels ( B , D ). Excitation was at 633 nm, and emission was collected from 650–850 nm. Scale bar, 10 µm.

    Journal: Sensors (Basel, Switzerland)

    Article Title: A Heptamethine Cyanine-Based Near-Infrared Optical Sensor for Copper(II) Detection in Aqueous Solutions and Living Cells

    doi: 10.3390/s26010130

    Figure Lengend Snippet: Confocal microscopy images of WS1 fibroblast cells. Bright-field image ( A ) and confocal fluorescence image ( B ) of WS1 cells incubated with IRPhen (10 µM) for 30 min. Bright-field image ( C ) and confocal fluorescence image ( D ) of cells pretreated with Cu 2+ (10 µM) for 8 h, followed by incubation with IRPhen (10 µM) for 30 min; ( E ) Quantitative bar graph showing the corresponding fluorescence intensities of panels ( B , D ). Excitation was at 633 nm, and emission was collected from 650–850 nm. Scale bar, 10 µm.

    Article Snippet: Human skin primary fibroblast cells (WS1) purchased from American Type Culture Collection (ATCC, Manassas, VA, USA) were used in this study.

    Techniques: Confocal Microscopy, Fluorescence, Incubation

    Evaluation of the IC 50 values of compound A determined for ASC52-telo cells and HDFa cells in 48- and 72-hour cell cultures.

    Journal: Cancer Management and Research

    Article Title: Potential of Using New Indole- and Benzimidazo[1,2-C]quinazolines in Anticancer Therapy Based on Mesenchymal Stem Cells

    doi: 10.2147/CMAR.S516593

    Figure Lengend Snippet: Evaluation of the IC 50 values of compound A determined for ASC52-telo cells and HDFa cells in 48- and 72-hour cell cultures.

    Article Snippet: Human skin fibroblast cell line (HDFa) (ATCC, PCS-201-012, Primary Dermal Fibroblast; Normal, Human, Adult) - a normal, adherent, skin cell line with research applications in responding to pathogens, skin aging, wound healing, gene delivery and skin diseases including scleroderma.

    Techniques:

    Evaluation of the IC 50 values of compound B determined for ASC52-telo cells and HDFa cells in 48- and 72-hour cell cultures.

    Journal: Cancer Management and Research

    Article Title: Potential of Using New Indole- and Benzimidazo[1,2-C]quinazolines in Anticancer Therapy Based on Mesenchymal Stem Cells

    doi: 10.2147/CMAR.S516593

    Figure Lengend Snippet: Evaluation of the IC 50 values of compound B determined for ASC52-telo cells and HDFa cells in 48- and 72-hour cell cultures.

    Article Snippet: Human skin fibroblast cell line (HDFa) (ATCC, PCS-201-012, Primary Dermal Fibroblast; Normal, Human, Adult) - a normal, adherent, skin cell line with research applications in responding to pathogens, skin aging, wound healing, gene delivery and skin diseases including scleroderma.

    Techniques: