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dermal fibroblast hs68 cell line  (ATCC)


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    Structured Review

    ATCC dermal fibroblast hs68 cell line
    Dermal Fibroblast Hs68 Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 637 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dermal fibroblast hs68 cell line/product/ATCC
    Average 96 stars, based on 637 article reviews
    dermal fibroblast hs68 cell line - by Bioz Stars, 2026-03
    96/100 stars

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    96
    ATCC dermal fibroblast hs68 cell line
    Dermal Fibroblast Hs68 Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dermal fibroblast hs68 cell line/product/ATCC
    Average 96 stars, based on 1 article reviews
    dermal fibroblast hs68 cell line - by Bioz Stars, 2026-03
    96/100 stars
      Buy from Supplier

    96
    ATCC dermal fibroblast cell line hs68
    Dermal Fibroblast Cell Line Hs68, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dermal fibroblast cell line hs68/product/ATCC
    Average 96 stars, based on 1 article reviews
    dermal fibroblast cell line hs68 - by Bioz Stars, 2026-03
    96/100 stars
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    96
    ATCC hs68 human dermal fibroblast cell line
    Effects of 10E-PDA on inhibiting melanogenesis in α-MSH-stimulated B16F10 melanoma cells. ( a ) B16F10, ( b ) <t>HS68,</t> and ( c ) HaCaT cells were treated with increasing concentrations of 10E-PDA (1–100 μM) for 24 h, after which cell viability was assessed (n = 4 per group). ( d , e ) B16F10 cells were pretreated with different concentrations of 10E-PDA (1–15 μM) or kojic acid (30 μM) for 1 h, followed by exposure to α-MSH (500 nM) for 6 days to measure melanin content ( d ) or for 3 days to examine tyrosinase activity ( e ). In both panels, the white bar represents the untreated control group without α-MSH stimulation, the black bar represents the α-MSH-stimulated control group, and the dark gray bars indicate the 10E-PDA-treated groups under α-MSH stimulation. In panel ( e ), the light gray bar represents the positive control group treated with kojic acid under α-MSH stimulation. Data are shown as mean ± SEM. ### p < 0.001 compared with the untreated control group, and * p < 0.05, ** p < 0.01, *** p < 0.001 compared with the α-MSH-treated group.
    Hs68 Human Dermal Fibroblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hs68 human dermal fibroblast cell line/product/ATCC
    Average 96 stars, based on 1 article reviews
    hs68 human dermal fibroblast cell line - by Bioz Stars, 2026-03
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    90
    BioResource International Inc human diploid dermal fibroblast hs68 cell line
    Changes in <t>Hs68</t> cell characteristics in the presence of CAP. Hs68 cell characteristics were examined following treatment of cells with different CAP concentrations (A) Cell viability, (B) migration (cells were also treated with MMC and TNF-α) and (C) percentage closure based on the cell migration assay were determined. (D) Relative mRNA levels of IL-6 in Hs68 cells treated with TNF-α and CAP. Scale bar, 500 µm. **P<0.01, ****P<0.0001. CAP, capsaicin; IL-6, interleukin 6; MMC, mitomycin C; TNF-α, tumor necrosis factor-α.
    Human Diploid Dermal Fibroblast Hs68 Cell Line, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human diploid dermal fibroblast hs68 cell line/product/BioResource International Inc
    Average 90 stars, based on 1 article reviews
    human diploid dermal fibroblast hs68 cell line - by Bioz Stars, 2026-03
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    90
    BioResource International Inc human diploid dermal fibroblast hs68 cell line (passage 19)
    Changes in <t>Hs68</t> cell characteristics in the presence of CAP. Hs68 cell characteristics were examined following treatment of cells with different CAP concentrations (A) Cell viability, (B) migration (cells were also treated with MMC and TNF-α) and (C) percentage closure based on the cell migration assay were determined. (D) Relative mRNA levels of IL-6 in Hs68 cells treated with TNF-α and CAP. Scale bar, 500 µm. **P<0.01, ****P<0.0001. CAP, capsaicin; IL-6, interleukin 6; MMC, mitomycin C; TNF-α, tumor necrosis factor-α.
    Human Diploid Dermal Fibroblast Hs68 Cell Line (Passage 19), supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human diploid dermal fibroblast hs68 cell line (passage 19)/product/BioResource International Inc
    Average 90 stars, based on 1 article reviews
    human diploid dermal fibroblast hs68 cell line (passage 19) - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

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    Effects of 10E-PDA on inhibiting melanogenesis in α-MSH-stimulated B16F10 melanoma cells. ( a ) B16F10, ( b ) HS68, and ( c ) HaCaT cells were treated with increasing concentrations of 10E-PDA (1–100 μM) for 24 h, after which cell viability was assessed (n = 4 per group). ( d , e ) B16F10 cells were pretreated with different concentrations of 10E-PDA (1–15 μM) or kojic acid (30 μM) for 1 h, followed by exposure to α-MSH (500 nM) for 6 days to measure melanin content ( d ) or for 3 days to examine tyrosinase activity ( e ). In both panels, the white bar represents the untreated control group without α-MSH stimulation, the black bar represents the α-MSH-stimulated control group, and the dark gray bars indicate the 10E-PDA-treated groups under α-MSH stimulation. In panel ( e ), the light gray bar represents the positive control group treated with kojic acid under α-MSH stimulation. Data are shown as mean ± SEM. ### p < 0.001 compared with the untreated control group, and * p < 0.05, ** p < 0.01, *** p < 0.001 compared with the α-MSH-treated group.

    Journal: Antioxidants

    Article Title: 10(E)-Pentadecenoic Acid Inhibits Melanogenesis Partly Through Suppressing the Intracellular MITF/Tyrosinase Axis

    doi: 10.3390/antiox13121547

    Figure Lengend Snippet: Effects of 10E-PDA on inhibiting melanogenesis in α-MSH-stimulated B16F10 melanoma cells. ( a ) B16F10, ( b ) HS68, and ( c ) HaCaT cells were treated with increasing concentrations of 10E-PDA (1–100 μM) for 24 h, after which cell viability was assessed (n = 4 per group). ( d , e ) B16F10 cells were pretreated with different concentrations of 10E-PDA (1–15 μM) or kojic acid (30 μM) for 1 h, followed by exposure to α-MSH (500 nM) for 6 days to measure melanin content ( d ) or for 3 days to examine tyrosinase activity ( e ). In both panels, the white bar represents the untreated control group without α-MSH stimulation, the black bar represents the α-MSH-stimulated control group, and the dark gray bars indicate the 10E-PDA-treated groups under α-MSH stimulation. In panel ( e ), the light gray bar represents the positive control group treated with kojic acid under α-MSH stimulation. Data are shown as mean ± SEM. ### p < 0.001 compared with the untreated control group, and * p < 0.05, ** p < 0.01, *** p < 0.001 compared with the α-MSH-treated group.

    Article Snippet: The B16F10 murine melanoma cell line and Hs68 human dermal fibroblast cell line were purchased from the American Type Culture Collection (ATCC, Rockville, MD, USA).

    Techniques: Activity Assay, Control, Positive Control

    Changes in Hs68 cell characteristics in the presence of CAP. Hs68 cell characteristics were examined following treatment of cells with different CAP concentrations (A) Cell viability, (B) migration (cells were also treated with MMC and TNF-α) and (C) percentage closure based on the cell migration assay were determined. (D) Relative mRNA levels of IL-6 in Hs68 cells treated with TNF-α and CAP. Scale bar, 500 µm. **P<0.01, ****P<0.0001. CAP, capsaicin; IL-6, interleukin 6; MMC, mitomycin C; TNF-α, tumor necrosis factor-α.

    Journal: Molecular Medicine Reports

    Article Title: Improvement of wound healing by capsaicin through suppression of the inflammatory response and amelioration of the repair process

    doi: 10.3892/mmr.2023.13042

    Figure Lengend Snippet: Changes in Hs68 cell characteristics in the presence of CAP. Hs68 cell characteristics were examined following treatment of cells with different CAP concentrations (A) Cell viability, (B) migration (cells were also treated with MMC and TNF-α) and (C) percentage closure based on the cell migration assay were determined. (D) Relative mRNA levels of IL-6 in Hs68 cells treated with TNF-α and CAP. Scale bar, 500 µm. **P<0.01, ****P<0.0001. CAP, capsaicin; IL-6, interleukin 6; MMC, mitomycin C; TNF-α, tumor necrosis factor-α.

    Article Snippet: The human diploid dermal fibroblast Hs68 cell line (passage 19), which is frequently used in dermal research and has the characteristics of primary dermal fibroblasts , was purchased from the Bioresource Collection and Research Center in the Food Industry Research and Development Institute (Hsinchu, Taiwan).

    Techniques: Migration, Cell Migration Assay