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human skin fibroblast cell line bj  (ATCC)


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    Structured Review

    ATCC human skin fibroblast cell line bj
    Viability of human skin <t>fibroblasts</t> (BJ) treated with chitosan films for 24 h at 37 °C (n = 6, * p < 0.05).
    Human Skin Fibroblast Cell Line Bj, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1783 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+skin+fibroblast+cell+line+bj/BJ/pmc13208214-58-1-12
    Average 99 stars, based on 1783 article reviews
    human skin fibroblast cell line bj - by Bioz Stars, 2026-09
    99/100 stars

    Images

    1) Product Images from "Green Chitosan Bioplastics: How the Filler Impacts the Biological Activity and the Biodegradability?"

    Article Title: Green Chitosan Bioplastics: How the Filler Impacts the Biological Activity and the Biodegradability?

    Journal: Materials

    doi: 10.3390/ma19102167

    Viability of human skin fibroblasts (BJ) treated with chitosan films for 24 h at 37 °C (n = 6, * p < 0.05).
    Figure Legend Snippet: Viability of human skin fibroblasts (BJ) treated with chitosan films for 24 h at 37 °C (n = 6, * p < 0.05).

    Techniques Used:

    Related Articles

    Cell Culture:

    Article Title: Matrix metalloproteinases inactivate the proinflammatory functions of secreted moonlighting tryptophanyl-tRNA synthetase
    Article Snippet: Protein concentrations were determined by bicinchoninic acid assay (Thermo Fisher Scientific). .. The human skin fibroblast cell line BJ (ATCC, catalog number CRL-2522) was cultured in Dulbecco's modified Eagle's medium (DMEM), 4.5 g/liter glucose, 10% (v/v) Cosmic calf serum (CCS; Hyclone), 50 μg/ml streptomycin, and 50 units/ml penicillin. .. Human primary umbilical vein endothelial cells (HUVECs) (Lonza, catalog number C2519A) were cultured in vascular cell basal medium plus Endothelial Cell Growth kit-VEGF (both from ATCC).

    Article Title: Role of Ciminalum-4-thiazolidinone Hybrids in Molecular NF-κB Dependent Pathways.
    Article Snippet: .. Cell Culture and Treatment The human epithelial lung carcinoma A549 (ATCC CCL-185) and the human skin fibroblast cell line BJ (ATCC CRL-2522) were supplied by the American Type Culture Collection (ATCC, distributor: LG Standards, Łomianki, Poland). ..

    Modification:

    Article Title: Matrix metalloproteinases inactivate the proinflammatory functions of secreted moonlighting tryptophanyl-tRNA synthetase
    Article Snippet: Protein concentrations were determined by bicinchoninic acid assay (Thermo Fisher Scientific). .. The human skin fibroblast cell line BJ (ATCC, catalog number CRL-2522) was cultured in Dulbecco's modified Eagle's medium (DMEM), 4.5 g/liter glucose, 10% (v/v) Cosmic calf serum (CCS; Hyclone), 50 μg/ml streptomycin, and 50 units/ml penicillin. .. Human primary umbilical vein endothelial cells (HUVECs) (Lonza, catalog number C2519A) were cultured in vascular cell basal medium plus Endothelial Cell Growth kit-VEGF (both from ATCC).



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    Evaluation of the effects of the RVs and CVs on H 2 O 2 -induced reactive oxygen species (ROS) and MDA production levels in <t>fibroblast</t> <t>BJ-5TA</t> cells ( A , B ) and differentiated C2C12 ( C , D ) cells. The data points represent the averages ±SD of three independent experiments in duplicate. All data sets were analyzed by one-way ANOVA followed by Tukey’s post hoc test. Different lowercase letters indicate a significant difference ( p < 0.05) between different treatments. Control: untreated cells. RVs: rosemary vesicles; CVs: coffee vesicles. 7.8 ×10 6 vesicles/mL and 39 ×10 6 vesicles/mL correspond to 0.1 and 0.5 mg nanovesicles/mL.
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    Evaluation of the effects of the RVs and CVs on H 2 O 2 -induced reactive oxygen species (ROS) and MDA production levels in <t>fibroblast</t> <t>BJ-5TA</t> cells ( A , B ) and differentiated C2C12 ( C , D ) cells. The data points represent the averages ±SD of three independent experiments in duplicate. All data sets were analyzed by one-way ANOVA followed by Tukey’s post hoc test. Different lowercase letters indicate a significant difference ( p < 0.05) between different treatments. Control: untreated cells. RVs: rosemary vesicles; CVs: coffee vesicles. 7.8 ×10 6 vesicles/mL and 39 ×10 6 vesicles/mL correspond to 0.1 and 0.5 mg nanovesicles/mL.
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    Evaluation of the effects of the RVs and CVs on H 2 O 2 -induced reactive oxygen species (ROS) and MDA production levels in <t>fibroblast</t> <t>BJ-5TA</t> cells ( A , B ) and differentiated C2C12 ( C , D ) cells. The data points represent the averages ±SD of three independent experiments in duplicate. All data sets were analyzed by one-way ANOVA followed by Tukey’s post hoc test. Different lowercase letters indicate a significant difference ( p < 0.05) between different treatments. Control: untreated cells. RVs: rosemary vesicles; CVs: coffee vesicles. 7.8 ×10 6 vesicles/mL and 39 ×10 6 vesicles/mL correspond to 0.1 and 0.5 mg nanovesicles/mL.
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    Image Search Results


    Viability of human skin fibroblasts (BJ) treated with chitosan films for 24 h at 37 °C (n = 6, * p < 0.05).

    Journal: Materials

    Article Title: Green Chitosan Bioplastics: How the Filler Impacts the Biological Activity and the Biodegradability?

    doi: 10.3390/ma19102167

    Figure Lengend Snippet: Viability of human skin fibroblasts (BJ) treated with chitosan films for 24 h at 37 °C (n = 6, * p < 0.05).

    Article Snippet: The human skin fibroblast cell line BJ (CRL-2522) was purchased from the American Type Culture Collection ATCC (Manassas, VA, USA).

    Techniques:

    Evaluation of the effects of the RVs and CVs on H 2 O 2 -induced reactive oxygen species (ROS) and MDA production levels in fibroblast BJ-5TA cells ( A , B ) and differentiated C2C12 ( C , D ) cells. The data points represent the averages ±SD of three independent experiments in duplicate. All data sets were analyzed by one-way ANOVA followed by Tukey’s post hoc test. Different lowercase letters indicate a significant difference ( p < 0.05) between different treatments. Control: untreated cells. RVs: rosemary vesicles; CVs: coffee vesicles. 7.8 ×10 6 vesicles/mL and 39 ×10 6 vesicles/mL correspond to 0.1 and 0.5 mg nanovesicles/mL.

    Journal: NPJ Science of Food

    Article Title: From rosemary and coffee to bioactive nanovesicles: exploring new frontiers in food functional ingredients

    doi: 10.1038/s41538-026-00723-9

    Figure Lengend Snippet: Evaluation of the effects of the RVs and CVs on H 2 O 2 -induced reactive oxygen species (ROS) and MDA production levels in fibroblast BJ-5TA cells ( A , B ) and differentiated C2C12 ( C , D ) cells. The data points represent the averages ±SD of three independent experiments in duplicate. All data sets were analyzed by one-way ANOVA followed by Tukey’s post hoc test. Different lowercase letters indicate a significant difference ( p < 0.05) between different treatments. Control: untreated cells. RVs: rosemary vesicles; CVs: coffee vesicles. 7.8 ×10 6 vesicles/mL and 39 ×10 6 vesicles/mL correspond to 0.1 and 0.5 mg nanovesicles/mL.

    Article Snippet: hTERT-immortalized human skin fibroblasts BJ-5TA cell line was bought from ATCC (ATCC (CRL-4001 TM), from LGC Standards, Milan, Italy), cultured in DMEM high glucose and Medium 199 (4:1 ratio) with stable L-glutamine supplemented with 10% FBS, 100 U/mL penicillin, 100 μg/mL streptomycin and incubated at 37 °C under a 5% CO 2 atmosphere.

    Techniques: Control