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normal mouse fibroblast l929 cells  (Boster Bio)


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    Boster Bio normal mouse fibroblast l929 cells
    Normal Mouse Fibroblast L929 Cells, supplied by Boster Bio, 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/product/normal+mouse+fibroblast+l929+cells/murine+fibroblast+l929+cells/pmc06149443-143-10-18
    Average 90 stars, based on 1 article reviews
    normal mouse fibroblast l929 cells - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    In Vitro:

    Article Title: Novel organophosphorus aminopyrimidines as unique structural DNA-targeting membrane active inhibitors towards drug-resistant methicillin-resistant Staphylococcus aureus †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8md00301g
    Article Snippet: .. 28 The active molecule 2c was further examined for its cytotoxic properties against normal mouse fibroblast L929 cells (Boster Biological Technology Co. Ltd, Tianjin, China). shows the in vitro cytotoxicity of compound 2c against L929 cells which was evaluated by the MTT assay. ..

    MTT Assay:

    Article Title: Novel organophosphorus aminopyrimidines as unique structural DNA-targeting membrane active inhibitors towards drug-resistant methicillin-resistant Staphylococcus aureus †Electronic supplementary information (ESI) available. See DOI: 10.1039/c8md00301g
    Article Snippet: .. 28 The active molecule 2c was further examined for its cytotoxic properties against normal mouse fibroblast L929 cells (Boster Biological Technology Co. Ltd, Tianjin, China). shows the in vitro cytotoxicity of compound 2c against L929 cells which was evaluated by the MTT assay. ..



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    The MTT assay results and effects of indicated concentrations of bare and functionalized ZnO NPs on the ( A ) Caco-2 cells and ( B ) <t>L929</t> cell viability. ( C ) the effect of different concentrations of biochemically synthetized ZnO NPs against the Caco-2 cell line. The values are expressed as mean ± SD values of three independent experiments ( n = 3); * p < 0.001 compared to bare ZnO NPs (ANOVA).
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    Image Search Results


    Effect of royal jelly (RJ) on normal cells. L929 and PBMC were used as models of normal cells. The MTT assay indicated that RJ has no cytotoxic effect on L929 and PBMC cells (A). Analysis of apoptosis using Annexin-V/PI staining and flow cytometry revealed that RJ has no significant apoptotic effect on normal cells (B). Hemolytic activity evolution suggested that the hemolysis rate decreases when RJ concentration increases (C). The values are given as the mean SD of three independent experiments. * P ≤0.05 represents significant statistical changes from the control sample

    Journal: Iranian Journal of Basic Medical Sciences

    Article Title: Royal jelly induces ROS-mediated apoptosis in acute lymphoblastic leukemia (ALL)-derived Nalm-6 cells: Shedding light on novel therapeutic approaches for ALL

    doi: 10.22038/IJBMS.2024.76261.16498

    Figure Lengend Snippet: Effect of royal jelly (RJ) on normal cells. L929 and PBMC were used as models of normal cells. The MTT assay indicated that RJ has no cytotoxic effect on L929 and PBMC cells (A). Analysis of apoptosis using Annexin-V/PI staining and flow cytometry revealed that RJ has no significant apoptotic effect on normal cells (B). Hemolytic activity evolution suggested that the hemolysis rate decreases when RJ concentration increases (C). The values are given as the mean SD of three independent experiments. * P ≤0.05 represents significant statistical changes from the control sample

    Article Snippet: Cell culture and treatment Acute Lymphoblastic Leukemia cell line (Nalm-6) and normal mouse fibroblast cell line (L929) were purchased from the Pasteur Institute collection (Tehran, Iran).

    Techniques: MTT Assay, Staining, Flow Cytometry, Activity Assay, Concentration Assay, Control

    The MTT assay results and effects of indicated concentrations of bare and functionalized ZnO NPs on the ( A ) Caco-2 cells and ( B ) L929 cell viability. ( C ) the effect of different concentrations of biochemically synthetized ZnO NPs against the Caco-2 cell line. The values are expressed as mean ± SD values of three independent experiments ( n = 3); * p < 0.001 compared to bare ZnO NPs (ANOVA).

    Journal: International Journal of Molecular Sciences

    Article Title: Comparison Study of Cytotoxicity of Bare and Functionalized Zinc Oxide Nanoparticles

    doi: 10.3390/ijms22179529

    Figure Lengend Snippet: The MTT assay results and effects of indicated concentrations of bare and functionalized ZnO NPs on the ( A ) Caco-2 cells and ( B ) L929 cell viability. ( C ) the effect of different concentrations of biochemically synthetized ZnO NPs against the Caco-2 cell line. The values are expressed as mean ± SD values of three independent experiments ( n = 3); * p < 0.001 compared to bare ZnO NPs (ANOVA).

    Article Snippet: The L929 normal mouse fibroblast cells and Caco-2 from human colon were obtained from the European Collection of Authenticated Cell Cultures.

    Techniques: MTT Assay

    LDH leakage level of Caco-2 and L929 cells treated with different concentrations of ( A ) chemically, ( B ) biochemically and ( C ) intracellularly synthetized ZnO NPs. The values are expressed as mean ± SD values of three independent experiments ( n = 3); * p < 0.001 (ANOVA).

    Journal: International Journal of Molecular Sciences

    Article Title: Comparison Study of Cytotoxicity of Bare and Functionalized Zinc Oxide Nanoparticles

    doi: 10.3390/ijms22179529

    Figure Lengend Snippet: LDH leakage level of Caco-2 and L929 cells treated with different concentrations of ( A ) chemically, ( B ) biochemically and ( C ) intracellularly synthetized ZnO NPs. The values are expressed as mean ± SD values of three independent experiments ( n = 3); * p < 0.001 (ANOVA).

    Article Snippet: The L929 normal mouse fibroblast cells and Caco-2 from human colon were obtained from the European Collection of Authenticated Cell Cultures.

    Techniques:

    SEM analysis showing the morphology changes in L929 cells after the bare and functionalized ZnO NPs treatement. ( A ) control sample and L929 cells after the ( B ) extracellularly, ( C ) phytochemically, ( D ) intracellularly, ( E ) chemically and ( F ) biochemically synthetized ZnO NPs’ exposure. The concentration of the used ZnO NPs was 6.25 μg/mL.

    Journal: International Journal of Molecular Sciences

    Article Title: Comparison Study of Cytotoxicity of Bare and Functionalized Zinc Oxide Nanoparticles

    doi: 10.3390/ijms22179529

    Figure Lengend Snippet: SEM analysis showing the morphology changes in L929 cells after the bare and functionalized ZnO NPs treatement. ( A ) control sample and L929 cells after the ( B ) extracellularly, ( C ) phytochemically, ( D ) intracellularly, ( E ) chemically and ( F ) biochemically synthetized ZnO NPs’ exposure. The concentration of the used ZnO NPs was 6.25 μg/mL.

    Article Snippet: The L929 normal mouse fibroblast cells and Caco-2 from human colon were obtained from the European Collection of Authenticated Cell Cultures.

    Techniques: Control, Concentration Assay

    Concentration-dependent ROS generation by bare and functionalized ZnO-NPs in ( A ) L929 and ( B ) Caco-2 cells. The values are expressed as mean ± SD values of three independent experiments ( n = 3); * p < 0.001 compared to bare ZnO NPs (ANOVA).

    Journal: International Journal of Molecular Sciences

    Article Title: Comparison Study of Cytotoxicity of Bare and Functionalized Zinc Oxide Nanoparticles

    doi: 10.3390/ijms22179529

    Figure Lengend Snippet: Concentration-dependent ROS generation by bare and functionalized ZnO-NPs in ( A ) L929 and ( B ) Caco-2 cells. The values are expressed as mean ± SD values of three independent experiments ( n = 3); * p < 0.001 compared to bare ZnO NPs (ANOVA).

    Article Snippet: The L929 normal mouse fibroblast cells and Caco-2 from human colon were obtained from the European Collection of Authenticated Cell Cultures.

    Techniques: Concentration Assay