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murine skeletal muscle derived myogenic progenitor cells (mmpcs)  (Jackson Laboratory)

 
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    Jackson Laboratory murine skeletal muscle derived myogenic progenitor cells (mmpcs)
    Murine Skeletal Muscle Derived Myogenic Progenitor Cells (Mmpcs), supplied by Jackson Laboratory, 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/murine+skeletal+muscle-derived+cells/murine+skeletal+muscle+derived+myogenic+progenitor+cells++mmpcs+/us12312600-18-2-24
    Average 90 stars, based on 1 article reviews
    murine skeletal muscle derived myogenic progenitor cells (mmpcs) - by Bioz Stars, 2026-10
    90/100 stars

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    other:

    Article Title: Generation of myogenic progenitor cell-derived smooth muscle cells for sphincter regeneration
    Article Snippet: Murine skeletal muscle-derived cells were obtained from skeletal muscle biopsies of Gt (ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/J, in short, TdTomato mice (Jackson Laboratory, ME, USA).



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    murine skeletal muscle derived myogenic progenitor cells (mmpcs)  (Jackson Laboratory)
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    Jackson Laboratory murine skeletal muscle derived myogenic progenitor cells (mmpcs)
    Murine Skeletal Muscle Derived Myogenic Progenitor Cells (Mmpcs), supplied by Jackson Laboratory, 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/murine+skeletal+muscle-derived+cells/murine+skeletal+muscle+derived+myogenic+progenitor+cells++mmpcs+/us12312600-18-2-24
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    murine skeletal muscle-derived cells  (Jackson Laboratory)
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    murine skeletal muscle derived c2c12 cell line  (ATCC)
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    ATCC murine skeletal muscle derived c2c12 cell line
    TNF, sphingomyelin, and oxidant signaling. (A) TNF-induced nSMase activity in myotubes, 5 min pretreatment of TNF (6 ng/ml, choline release, n =9), ⁎ P <0.05. (B) Increased oxidant activity in <t>C2C12</t> myotubes pretreated for 20 min with TNF (6 ng/ml) or C2-ceramide (10 µM). Measured by DCF fluorescence assay, each treatment was applied to 12-wells of cultured myotubes, the 5 brightest myotubes per well were analyzed, each data point is an average of these 5 myotubes (RFU=relative fluorescence units), ⁎ P <0.02 vs. untreated, paired comparison.
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    undifferentiated murine skeletal muscle derived c2c12 cells  (ATCC)
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    ATCC undifferentiated murine skeletal muscle derived c2c12 cells
    TNF, sphingomyelin, and oxidant signaling. (A) TNF-induced nSMase activity in myotubes, 5 min pretreatment of TNF (6 ng/ml, choline release, n =9), ⁎ P <0.05. (B) Increased oxidant activity in <t>C2C12</t> myotubes pretreated for 20 min with TNF (6 ng/ml) or C2-ceramide (10 µM). Measured by DCF fluorescence assay, each treatment was applied to 12-wells of cultured myotubes, the 5 brightest myotubes per well were analyzed, each data point is an average of these 5 myotubes (RFU=relative fluorescence units), ⁎ P <0.02 vs. untreated, paired comparison.
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    Image Search Results


    TNF, sphingomyelin, and oxidant signaling. (A) TNF-induced nSMase activity in myotubes, 5 min pretreatment of TNF (6 ng/ml, choline release, n =9), ⁎ P <0.05. (B) Increased oxidant activity in C2C12 myotubes pretreated for 20 min with TNF (6 ng/ml) or C2-ceramide (10 µM). Measured by DCF fluorescence assay, each treatment was applied to 12-wells of cultured myotubes, the 5 brightest myotubes per well were analyzed, each data point is an average of these 5 myotubes (RFU=relative fluorescence units), ⁎ P <0.02 vs. untreated, paired comparison.

    Journal: Redox Biology

    Article Title: Neutral sphingomyelinase-3 mediates TNF-stimulated oxidant activity in skeletal muscle

    doi: 10.1016/j.redox.2014.07.006

    Figure Lengend Snippet: TNF, sphingomyelin, and oxidant signaling. (A) TNF-induced nSMase activity in myotubes, 5 min pretreatment of TNF (6 ng/ml, choline release, n =9), ⁎ P <0.05. (B) Increased oxidant activity in C2C12 myotubes pretreated for 20 min with TNF (6 ng/ml) or C2-ceramide (10 µM). Measured by DCF fluorescence assay, each treatment was applied to 12-wells of cultured myotubes, the 5 brightest myotubes per well were analyzed, each data point is an average of these 5 myotubes (RFU=relative fluorescence units), ⁎ P <0.02 vs. untreated, paired comparison.

    Article Snippet: Myoblasts from the murine skeletal muscle-derived C2C12 cell line (American Type Culture Collection, Rockville, MD) were cultured as in Smith et al. .

    Techniques: Activity Assay, Fluorescence, Cell Culture, Comparison