Review




Structured Review

Korean Cell Line Bank hdf cell line ccd 986sk
In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF <t>(CCD‐986Sk)</t> cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.
Hdf Cell Line Ccd 986sk, supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hdf+cell+line/986sk+ccd/pmc13058775-249-1-11
Average 86 stars, based on 1 article reviews
hdf cell line ccd 986sk - by Bioz Stars, 2026-09
86/100 stars

Images

1) Product Images from "Skin‐Interfaced Therapeutic Patches for Wound Fluid Management and Transdermal Drug Delivery"

Article Title: Skin‐Interfaced Therapeutic Patches for Wound Fluid Management and Transdermal Drug Delivery

Journal: Advanced Healthcare Materials

doi: 10.1002/adhm.202504450

In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF (CCD‐986Sk) cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.
Figure Legend Snippet: In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF (CCD‐986Sk) cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.

Techniques Used: In Vitro, Fluorescence

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Image Search Results


Cell viability % efficiency of the green synthesized Ag/ZnO NCs. a Human malignant melanoma cells (A375), b Human dermal fibroblast cells (HDF)

Journal: Discover Nano

Article Title: Evaluation of the antivirulence and anticancer potential of green-synthesized silver/zinc oxide nanocomposites against methicillin-resistant Staphylococcus aureus and melanoma cells

doi: 10.1186/s11671-026-04444-6

Figure Lengend Snippet: Cell viability % efficiency of the green synthesized Ag/ZnO NCs. a Human malignant melanoma cells (A375), b Human dermal fibroblast cells (HDF)

Article Snippet: The human melanoma (A375) and human dermal fibroblast (HDF) cell lines, obtained from the Pasteur Institute (Tehran, Iran), were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium supplemented with 10% fetal bovine serum (FBS), 100 U/mL penicillin G, and 100 μg/mL streptomycin.

Techniques: Synthesized

In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF (CCD‐986Sk) cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Advanced Healthcare Materials

Article Title: Skin‐Interfaced Therapeutic Patches for Wound Fluid Management and Transdermal Drug Delivery

doi: 10.1002/adhm.202504450

Figure Lengend Snippet: In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF (CCD‐986Sk) cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: The HDF cell line CCD‐986Sk (RRID: CVCL_4200) was obtained from the Korean Cell Line Bank (KCLB, Seoul, South Korea) on August 2024 and was likewise confirmed to be free of contamination upon arrival.

Techniques: In Vitro, Fluorescence