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mouse myoblast cell line c2c12  (ATCC)


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    Structured Review

    ATCC mouse myoblast cell line c2c12
    Mouse Myoblast Cell Line C2c12, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 9251 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse myoblast cell line c2c12/product/ATCC
    Average 99 stars, based on 9251 article reviews
    mouse myoblast cell line c2c12 - by Bioz Stars, 2026-04
    99/100 stars

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    ATCC c2c12 cell line
    Yoda1‐induced sEV promotes myotube formation. (A) Representative optical field areas of 4‐day differentiating <t>C2C12</t> cells in control conditions (Ctrl; DM medium), treated with exogenous sEV derived from MB and MT cultures (cMB‐sEV and cMT‐sEV) or with exogenous sEV derived from Yoda1‐treated MB and MT cultures (yMB‐sEV and yMT‐sEV). Fluorescence images (DAPI staining) were overlaid on the corresponding bright‐field images. (B) The number of myotubes in each optical field (OF) was normalized to the average number of myotubes observed in Ctrl condition. For each experimental point, at least 40 randomly selected.
    C2c12 Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/c2c12 cell line/product/ATCC
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    ATCC c2c12 mouse myoblast cell lines
    Yoda1‐induced sEV promotes myotube formation. (A) Representative optical field areas of 4‐day differentiating <t>C2C12</t> cells in control conditions (Ctrl; DM medium), treated with exogenous sEV derived from MB and MT cultures (cMB‐sEV and cMT‐sEV) or with exogenous sEV derived from Yoda1‐treated MB and MT cultures (yMB‐sEV and yMT‐sEV). Fluorescence images (DAPI staining) were overlaid on the corresponding bright‐field images. (B) The number of myotubes in each optical field (OF) was normalized to the average number of myotubes observed in Ctrl condition. For each experimental point, at least 40 randomly selected.
    C2c12 Mouse Myoblast Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/c2c12 mouse myoblast cell lines/product/ATCC
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    ATCC murine myoblast cell line c2c12
    Yoda1‐induced sEV promotes myotube formation. (A) Representative optical field areas of 4‐day differentiating <t>C2C12</t> cells in control conditions (Ctrl; DM medium), treated with exogenous sEV derived from MB and MT cultures (cMB‐sEV and cMT‐sEV) or with exogenous sEV derived from Yoda1‐treated MB and MT cultures (yMB‐sEV and yMT‐sEV). Fluorescence images (DAPI staining) were overlaid on the corresponding bright‐field images. (B) The number of myotubes in each optical field (OF) was normalized to the average number of myotubes observed in Ctrl condition. For each experimental point, at least 40 randomly selected.
    Murine Myoblast Cell Line C2c12, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC c2c12 mouse myoblast cell line
    Yoda1‐induced sEV promotes myotube formation. (A) Representative optical field areas of 4‐day differentiating <t>C2C12</t> cells in control conditions (Ctrl; DM medium), treated with exogenous sEV derived from MB and MT cultures (cMB‐sEV and cMT‐sEV) or with exogenous sEV derived from Yoda1‐treated MB and MT cultures (yMB‐sEV and yMT‐sEV). Fluorescence images (DAPI staining) were overlaid on the corresponding bright‐field images. (B) The number of myotubes in each optical field (OF) was normalized to the average number of myotubes observed in Ctrl condition. For each experimental point, at least 40 randomly selected.
    C2c12 Mouse Myoblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/c2c12 mouse myoblast cell line/product/ATCC
    Average 99 stars, based on 1 article reviews
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    ATCC cell culture c2c12 myoblast cell line
    Yoda1‐induced sEV promotes myotube formation. (A) Representative optical field areas of 4‐day differentiating <t>C2C12</t> cells in control conditions (Ctrl; DM medium), treated with exogenous sEV derived from MB and MT cultures (cMB‐sEV and cMT‐sEV) or with exogenous sEV derived from Yoda1‐treated MB and MT cultures (yMB‐sEV and yMT‐sEV). Fluorescence images (DAPI staining) were overlaid on the corresponding bright‐field images. (B) The number of myotubes in each optical field (OF) was normalized to the average number of myotubes observed in Ctrl condition. For each experimental point, at least 40 randomly selected.
    Cell Culture C2c12 Myoblast Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC c2c12 myoblast cell lines
    Tobacco smoke and E‐cig vapor condensates activate the AHR pathway and alter mitochondrial respiration in cultured muscle cells. (a) <t>C2C12</t> myotubes were treated for 16 h without affecting cell viability. (b–d) mRNA expression of Ahr , Ahrr , and Cyp1a1 in treated myotubes. (e) Schematic overview of mitochondrial assay. (f, g) Mitochondrial respiration assessed using respirometry. Data analyzed using Kruskal‐Wallis test. N = 4–6 biological replicates per group. Error bars represent the standard deviation.
    C2c12 Myoblast Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/c2c12 myoblast cell lines/product/ATCC
    Average 99 stars, based on 1 article reviews
    c2c12 myoblast cell lines - by Bioz Stars, 2026-04
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    Image Search Results


    Yoda1‐induced sEV promotes myotube formation. (A) Representative optical field areas of 4‐day differentiating C2C12 cells in control conditions (Ctrl; DM medium), treated with exogenous sEV derived from MB and MT cultures (cMB‐sEV and cMT‐sEV) or with exogenous sEV derived from Yoda1‐treated MB and MT cultures (yMB‐sEV and yMT‐sEV). Fluorescence images (DAPI staining) were overlaid on the corresponding bright‐field images. (B) The number of myotubes in each optical field (OF) was normalized to the average number of myotubes observed in Ctrl condition. For each experimental point, at least 40 randomly selected.

    Journal: Journal of Cellular Physiology

    Article Title: PIEZO1 Channels Modulate the Small Extracellular Vesicle Release in C2C12 Cells

    doi: 10.1002/jcp.70155

    Figure Lengend Snippet: Yoda1‐induced sEV promotes myotube formation. (A) Representative optical field areas of 4‐day differentiating C2C12 cells in control conditions (Ctrl; DM medium), treated with exogenous sEV derived from MB and MT cultures (cMB‐sEV and cMT‐sEV) or with exogenous sEV derived from Yoda1‐treated MB and MT cultures (yMB‐sEV and yMT‐sEV). Fluorescence images (DAPI staining) were overlaid on the corresponding bright‐field images. (B) The number of myotubes in each optical field (OF) was normalized to the average number of myotubes observed in Ctrl condition. For each experimental point, at least 40 randomly selected.

    Article Snippet: Myoblasts derived from the C2C12 cell line (RRID: CVCL_0188, ATCC‐CRL‐1772, LCG Standards S.r.l, MI, Italy) were kept in growth media (GM) containing Dulbecco's Modified Eagle Medium‐High Glucose (DMEM, Sigma‐Aldrich, St. Louis, Missouri, USA), 20% Fetal Bovin Serum (FBS; EuroClone, Pero, MI, Italy), 4 mM l ‐Glutamine (EuroClone, Perom MI, Italy), 1% Penicillin‐Streptomycin (EuroClone, Pero, MI, Italy), at 37°C in humidified air containing 5% CO 2 .

    Techniques: Control, Derivative Assay, Fluorescence, Staining

    Tobacco smoke and E‐cig vapor condensates activate the AHR pathway and alter mitochondrial respiration in cultured muscle cells. (a) C2C12 myotubes were treated for 16 h without affecting cell viability. (b–d) mRNA expression of Ahr , Ahrr , and Cyp1a1 in treated myotubes. (e) Schematic overview of mitochondrial assay. (f, g) Mitochondrial respiration assessed using respirometry. Data analyzed using Kruskal‐Wallis test. N = 4–6 biological replicates per group. Error bars represent the standard deviation.

    Journal: Physiological Reports

    Article Title: E‐cigarette exposure impairs skeletal muscle mitochondrial function in male mice

    doi: 10.14814/phy2.70797

    Figure Lengend Snippet: Tobacco smoke and E‐cig vapor condensates activate the AHR pathway and alter mitochondrial respiration in cultured muscle cells. (a) C2C12 myotubes were treated for 16 h without affecting cell viability. (b–d) mRNA expression of Ahr , Ahrr , and Cyp1a1 in treated myotubes. (e) Schematic overview of mitochondrial assay. (f, g) Mitochondrial respiration assessed using respirometry. Data analyzed using Kruskal‐Wallis test. N = 4–6 biological replicates per group. Error bars represent the standard deviation.

    Article Snippet: C2C12 myoblast cell lines were obtained from ATCC (Cat. No. CRL‐1772) and cultured in Dulbecco's Modified Eagle Medium (DMEM, ThermoFisher, Cat. No. 10567022) supplemented with 10% fetal bovine serum and 1% penicillin/streptomycin, in standard conditions (37°C, 5% CO 2 ).

    Techniques: Cell Culture, Expressing, Standard Deviation