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bj normal human skin fibroblast cell lines  (ATCC)


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    ATCC bj normal human skin fibroblast cell lines
    Bj Normal Human Skin Fibroblast Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 476 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bj+normal+human+skin+fibroblast+cell+lines/Human+skin+fibroblast/pm39935420-17-12-23
    Average 95 stars, based on 476 article reviews
    bj normal human skin fibroblast cell lines - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Selisistat, a SIRT1 inhibitor, enhances paclitaxel activity in luminal and triple-negative breast cancer: in silico, in vitro, and in vivo studies.
    Article Snippet: .. the human t47D, McF7 Bc luminal a, MDa-MB-231, MDa-MB-468, Bt-549 tNBc and BJ normal human skin fibroblast cell lines were obtained from the american type culture collection (atcc) (Manassas, Va, Usa). the cells were cultured in the Dulbecco’s Modified eagle Medium (DMeM)/ham’s Nutrient Mixture F-12 medium (sigma) supplemented with 10% foetal bovine serum (FBs) (sigma), penicillin (100 units/ml) (sigma), streptomycin (100 μg/ml) (sigma) and incubated at 37 °c with 5% cO2. ..

    Modification:

    Article Title: Selisistat, a SIRT1 inhibitor, enhances paclitaxel activity in luminal and triple-negative breast cancer: in silico, in vitro, and in vivo studies.
    Article Snippet: .. the human t47D, McF7 Bc luminal a, MDa-MB-231, MDa-MB-468, Bt-549 tNBc and BJ normal human skin fibroblast cell lines were obtained from the american type culture collection (atcc) (Manassas, Va, Usa). the cells were cultured in the Dulbecco’s Modified eagle Medium (DMeM)/ham’s Nutrient Mixture F-12 medium (sigma) supplemented with 10% foetal bovine serum (FBs) (sigma), penicillin (100 units/ml) (sigma), streptomycin (100 μg/ml) (sigma) and incubated at 37 °c with 5% cO2. ..

    Incubation:

    Article Title: Selisistat, a SIRT1 inhibitor, enhances paclitaxel activity in luminal and triple-negative breast cancer: in silico, in vitro, and in vivo studies.
    Article Snippet: .. the human t47D, McF7 Bc luminal a, MDa-MB-231, MDa-MB-468, Bt-549 tNBc and BJ normal human skin fibroblast cell lines were obtained from the american type culture collection (atcc) (Manassas, Va, Usa). the cells were cultured in the Dulbecco’s Modified eagle Medium (DMeM)/ham’s Nutrient Mixture F-12 medium (sigma) supplemented with 10% foetal bovine serum (FBs) (sigma), penicillin (100 units/ml) (sigma), streptomycin (100 μg/ml) (sigma) and incubated at 37 °c with 5% cO2. ..

    Multiple Displacement Amplification:

    Article Title: Selisistat, a SIRT1 inhibitor, enhances paclitaxel activity in luminal and triple-negative breast cancer: in silico, in vitro, and in vivo studies
    Article Snippet: .. The human T47D, MCF7 BC luminal A, MDA-MB-231, MDA-MB-468, BT-549 TNBC and BJ normal human skin fibroblast cell lines were obtained from the American Type Culture Collection (ATCC) (Manassas, VA, USA). .. The cells were cultured in the Dulbecco’s Modified Eagle Medium (DMEM)/Ham’s Nutrient Mixture F-12 medium (Sigma) supplemented with 10% foetal bovine serum (FBS) (Sigma), penicillin (100 units/ml) (Sigma), streptomycin (100 μg/ml) (Sigma) and incubated at 37 °C with 5% CO 2 .



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    ATCC normal human skin fibroblast cell line bj
    Dose-effect analysis on MTS reduction by human normal BJ <t>fibroblasts</t> and by various human tumor cells (HT29 and HCT116 colon carcinoma, and DU145 prostate carcinoma) exposed to 64 Cu in the dose range of 2, 10, 20 and 40 MBq/mL for various time points: (A) 24 h; (B) 48 h; (C) 72 h. Results are presented as mean ± SEM for triplicate samples. 64 Cu effect was calculated as MTS reduction value (OD) for each sample of the triplicate divided by the mean value of MTS reduction in the non-treated controls.
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    ATCC normal human fibroblast cells bj
    Cellular uptake of polymer-coated iron oxide nanoparticles. ( A – D ) TEM micrographs show cellular uptake in HT1080 cells ( A , C ) and BJ <t>(fibroblast)</t> cells ( B , D ) after 24 h of exposure to 50 μg/mL Fe 2 O 3 nanoparticles ( A , B ) or Fe 2 O 3 @Co-PEG nanoparticles ( C , D ). The arrows indicate the presence of nanoparticles. N, cell nucleus. Scale bars in all panels: 2 μm. ( E – H ) ICP-MS measurements. Cellular concentration of Fe ( E , F ) and Co ( G , H ) in cells exposed to 50 μg/mL Fe 2 O 3 or Fe 2 O 3 @Co-PEG for 24 h determined by ICP-MS.
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    Image Search Results


    Dose-effect analysis on MTS reduction by human normal BJ fibroblasts and by various human tumor cells (HT29 and HCT116 colon carcinoma, and DU145 prostate carcinoma) exposed to 64 Cu in the dose range of 2, 10, 20 and 40 MBq/mL for various time points: (A) 24 h; (B) 48 h; (C) 72 h. Results are presented as mean ± SEM for triplicate samples. 64 Cu effect was calculated as MTS reduction value (OD) for each sample of the triplicate divided by the mean value of MTS reduction in the non-treated controls.

    Journal: Frontiers in Medicine

    Article Title: Modifications in cellular viability, DNA damage and stress responses inflicted in cancer cells by copper-64 ions

    doi: 10.3389/fmed.2023.1197846

    Figure Lengend Snippet: Dose-effect analysis on MTS reduction by human normal BJ fibroblasts and by various human tumor cells (HT29 and HCT116 colon carcinoma, and DU145 prostate carcinoma) exposed to 64 Cu in the dose range of 2, 10, 20 and 40 MBq/mL for various time points: (A) 24 h; (B) 48 h; (C) 72 h. Results are presented as mean ± SEM for triplicate samples. 64 Cu effect was calculated as MTS reduction value (OD) for each sample of the triplicate divided by the mean value of MTS reduction in the non-treated controls.

    Article Snippet: Three human tumors lines: HT29 (colon adenocarcinoma, ATCC HTB-38), HCT116 (colon carcinoma, ATCC CCL-247), DU145 (prostate carcinoma, ATCC HTB-81), and normal human skin fibroblast cell line BJ (ATCC CRL-2522) were cultivated according to the depositor’s proposed protocols (ATCC, American Tissue and Cell Collection) at 37°C and 5% CO 2 in DMEM culture medium (Gibco, ThermoFisher Scientific, Waltham, MA, US) supplemented with 10% FBS (Euroclone, Milan, Italy), and a stabilized Antibiotic Antimycotic Solution (100x) (Sigma, Saint Louis, MO, US) containing 10,000 units penicillin, 10 mg streptomycin and 25 μg Amphotericin B per mL.

    Techniques:

    Changes in the expression of stress genes triggered by the treatment of human normal BJ fibroblasts with 20 MBq/mL 64 Cu for 24 h. qRT-PCR results were presented as mean value of Fold Change (FC) ± SEM for 3 independent experiments. Only genes with significant expression changes (1.5 < FC < 0.7) were represented.

    Journal: Frontiers in Medicine

    Article Title: Modifications in cellular viability, DNA damage and stress responses inflicted in cancer cells by copper-64 ions

    doi: 10.3389/fmed.2023.1197846

    Figure Lengend Snippet: Changes in the expression of stress genes triggered by the treatment of human normal BJ fibroblasts with 20 MBq/mL 64 Cu for 24 h. qRT-PCR results were presented as mean value of Fold Change (FC) ± SEM for 3 independent experiments. Only genes with significant expression changes (1.5 < FC < 0.7) were represented.

    Article Snippet: Three human tumors lines: HT29 (colon adenocarcinoma, ATCC HTB-38), HCT116 (colon carcinoma, ATCC CCL-247), DU145 (prostate carcinoma, ATCC HTB-81), and normal human skin fibroblast cell line BJ (ATCC CRL-2522) were cultivated according to the depositor’s proposed protocols (ATCC, American Tissue and Cell Collection) at 37°C and 5% CO 2 in DMEM culture medium (Gibco, ThermoFisher Scientific, Waltham, MA, US) supplemented with 10% FBS (Euroclone, Milan, Italy), and a stabilized Antibiotic Antimycotic Solution (100x) (Sigma, Saint Louis, MO, US) containing 10,000 units penicillin, 10 mg streptomycin and 25 μg Amphotericin B per mL.

    Techniques: Expressing, Quantitative RT-PCR

    Cellular uptake of polymer-coated iron oxide nanoparticles. ( A – D ) TEM micrographs show cellular uptake in HT1080 cells ( A , C ) and BJ (fibroblast) cells ( B , D ) after 24 h of exposure to 50 μg/mL Fe 2 O 3 nanoparticles ( A , B ) or Fe 2 O 3 @Co-PEG nanoparticles ( C , D ). The arrows indicate the presence of nanoparticles. N, cell nucleus. Scale bars in all panels: 2 μm. ( E – H ) ICP-MS measurements. Cellular concentration of Fe ( E , F ) and Co ( G , H ) in cells exposed to 50 μg/mL Fe 2 O 3 or Fe 2 O 3 @Co-PEG for 24 h determined by ICP-MS.

    Journal: Nanomaterials

    Article Title: High-Dose Exposure to Polymer-Coated Iron Oxide Nanoparticles Elicits Autophagy-Dependent Ferroptosis in Susceptible Cancer Cells

    doi: 10.3390/nano13111719

    Figure Lengend Snippet: Cellular uptake of polymer-coated iron oxide nanoparticles. ( A – D ) TEM micrographs show cellular uptake in HT1080 cells ( A , C ) and BJ (fibroblast) cells ( B , D ) after 24 h of exposure to 50 μg/mL Fe 2 O 3 nanoparticles ( A , B ) or Fe 2 O 3 @Co-PEG nanoparticles ( C , D ). The arrows indicate the presence of nanoparticles. N, cell nucleus. Scale bars in all panels: 2 μm. ( E – H ) ICP-MS measurements. Cellular concentration of Fe ( E , F ) and Co ( G , H ) in cells exposed to 50 μg/mL Fe 2 O 3 or Fe 2 O 3 @Co-PEG for 24 h determined by ICP-MS.

    Article Snippet: The human fibrosarcoma cell line (HT1080) and normal human fibroblast cells (BJ) were obtained from American Type Culture Collection (ATCC).

    Techniques: Polymer, Concentration Assay