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dermal fibroblasts hdfs normal human dermal fibroblast hdf cells  (PromoCell)


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    PromoCell dermal fibroblasts hdfs normal human dermal fibroblast hdf cells
    Dermal Fibroblasts Hdfs Normal Human Dermal Fibroblast Hdf Cells, supplied by PromoCell, used in various techniques. Bioz Stars score: 98/100, based on 931 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dermal fibroblasts hdfs normal human dermal fibroblast hdf cells/product/PromoCell
    Average 98 stars, based on 931 article reviews
    dermal fibroblasts hdfs normal human dermal fibroblast hdf cells - by Bioz Stars, 2026-03
    98/100 stars

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    In vitro wound-healing activity of Ep EVs-LL37 evaluated using a cell migration assay. LL37, Ep EVs, or Ep EVs-LL37 (5 and 10 µg/mL) were treated to HDF cells and observed the cell migration. ( a ) Representative light microscope images showing the cell-free wound area at different time points. ( b ) Quantification of wound area (%) was performed using ImageJ software. The open wound area (%) was plotted against hours post-treatment (hpt). Data were compared with the negative control (NC) group at each time point and reported as means ± SEM. Statistical analysis was performed using two-way ANOVA followed by Dunnett’s multiple comparison test. (Scale bar = 100 μm; * = p < 0.05. ** = p < 0.01, *** = p < 0.001, **** = p < 0.0001).

    Journal: Scientific Reports

    Article Title: Cathelicidin LL37-loaded extracellular vesicles from Edwardsiella piscicida promote antibacterial and wound-healing activity

    doi: 10.1038/s41598-025-28377-9

    Figure Lengend Snippet: In vitro wound-healing activity of Ep EVs-LL37 evaluated using a cell migration assay. LL37, Ep EVs, or Ep EVs-LL37 (5 and 10 µg/mL) were treated to HDF cells and observed the cell migration. ( a ) Representative light microscope images showing the cell-free wound area at different time points. ( b ) Quantification of wound area (%) was performed using ImageJ software. The open wound area (%) was plotted against hours post-treatment (hpt). Data were compared with the negative control (NC) group at each time point and reported as means ± SEM. Statistical analysis was performed using two-way ANOVA followed by Dunnett’s multiple comparison test. (Scale bar = 100 μm; * = p < 0.05. ** = p < 0.01, *** = p < 0.001, **** = p < 0.0001).

    Article Snippet: A cell migration assay was carried out using HDF cells (PCS-201-010TM, ATCC, Manassas, VA, USA) to assess the wound-healing effects of Ep EVs-LL37, based on the method described by Edirisinghe et al. .

    Techniques: In Vitro, Activity Assay, Cell Migration Assay, Migration, Light Microscopy, Software, Negative Control, Comparison