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murine fibroblast l929 cells  (ATCC)


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    Structured Review

    ATCC murine fibroblast l929 cells
    Murine Fibroblast L929 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3264 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/murine fibroblast l929 cells/product/ATCC
    Average 99 stars, based on 3264 article reviews
    murine fibroblast l929 cells - by Bioz Stars, 2026-03
    99/100 stars

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    ATCC murine fibroblast nih 3t3 cells
    Intracellular activity of sorangicins against S. aureus Newman in A549 ( A ) and NIH <t>3T3</t> ( B ) cells. At 1.75 hours post infection, cells were washed once and treated with different concentrations of rifampicin (RIF), sorangicin A (SorA), neosorangicin A (NeoSorA), or with 0.1% ( v/v ) methanol (control) in the presence of 10 µg mL −1 gentamicin. Reduction of bacterial burden was evaluated 24 hours post infection by CFU (colony-forming unit) counting. Limit of detection (LoD) is 10 1 CFU. Horizontal lines represent mean values of at least three independent biological experiments. Statistical analysis was performed by one-way ANOVA with Dunnett’s multiple comparison test. p < 0.05: *, p < 0.0001: ****.
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    ATCC murine nih 3t3 fibroblasts
    Intracellular activity of sorangicins against S. aureus Newman in A549 ( A ) and NIH <t>3T3</t> ( B ) cells. At 1.75 hours post infection, cells were washed once and treated with different concentrations of rifampicin (RIF), sorangicin A (SorA), neosorangicin A (NeoSorA), or with 0.1% ( v/v ) methanol (control) in the presence of 10 µg mL −1 gentamicin. Reduction of bacterial burden was evaluated 24 hours post infection by CFU (colony-forming unit) counting. Limit of detection (LoD) is 10 1 CFU. Horizontal lines represent mean values of at least three independent biological experiments. Statistical analysis was performed by one-way ANOVA with Dunnett’s multiple comparison test. p < 0.05: *, p < 0.0001: ****.
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    Intracellular activity of sorangicins against S. aureus Newman in A549 ( A ) and NIH 3T3 ( B ) cells. At 1.75 hours post infection, cells were washed once and treated with different concentrations of rifampicin (RIF), sorangicin A (SorA), neosorangicin A (NeoSorA), or with 0.1% ( v/v ) methanol (control) in the presence of 10 µg mL −1 gentamicin. Reduction of bacterial burden was evaluated 24 hours post infection by CFU (colony-forming unit) counting. Limit of detection (LoD) is 10 1 CFU. Horizontal lines represent mean values of at least three independent biological experiments. Statistical analysis was performed by one-way ANOVA with Dunnett’s multiple comparison test. p < 0.05: *, p < 0.0001: ****.

    Journal: bioRxiv

    Article Title: Structure Elucidation, Biosynthesis and Biological Evaluation of Neosorangicin A, a Member of the Sorangicin Family

    doi: 10.64898/2026.01.26.701680

    Figure Lengend Snippet: Intracellular activity of sorangicins against S. aureus Newman in A549 ( A ) and NIH 3T3 ( B ) cells. At 1.75 hours post infection, cells were washed once and treated with different concentrations of rifampicin (RIF), sorangicin A (SorA), neosorangicin A (NeoSorA), or with 0.1% ( v/v ) methanol (control) in the presence of 10 µg mL −1 gentamicin. Reduction of bacterial burden was evaluated 24 hours post infection by CFU (colony-forming unit) counting. Limit of detection (LoD) is 10 1 CFU. Horizontal lines represent mean values of at least three independent biological experiments. Statistical analysis was performed by one-way ANOVA with Dunnett’s multiple comparison test. p < 0.05: *, p < 0.0001: ****.

    Article Snippet: Human alveolar epithelial A549 cells (ATCC CCL-185) and murine fibroblast NIH 3T3 cells (ATCC CRL-1658), obtained from the American Type Culture Collection, were cultured in DMEM with 4.5 g/L glucose, 10% fetal bovine serum, 2 mM L -glutamine, 1mM sodium pyruvate and 1% non-essential amino acids at 37 °C and 7.5% CO 2 .

    Techniques: Activity Assay, Infection, Control, Comparison