Abstract
We describe the immunostaining methods we commonly use to detect the more robust cell markers identifying the various cell populations obtained by the enzymatic and or mechanical dissociation of muscle satellite cells: CD34, m-Cadherin, and Pax7, self-renewing muscle stem cells expressing CXCR4 and β1-integrin, populations of proliferative myogenic progenitor cells expressing, Pax3, Pax7, Myf5, MyoD1, and desmin, differentiating myoblasts expressing myogenin and eMHC, and the CD45 expressing leukocyte lineage cells that infiltrate injured and regenerating skeletal muscle.
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References
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Acknowledgments
We thank the National Institutes of Health, National Institute on Aging (R01 AG027252 and K01 AR050515 to I.M.C.), the Stem Cell Research Foundation (Maryland, to I.M.C.), and the Harvard Stem Cell Institute (Cambridge, MA, to A.J.W.) for recent and current funding of these endeavors.
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Conboy, M.J., Cerletti, M., Wagers, A.J., Conboy, I.M. (2010). Immuno-Analysis and FACS Sorting of Adult Muscle Fiber-Associated Stem/Precursor Cells. In: Conboy, I., Schaffer, D., Barcellos-Hoff, M., Li, S. (eds) Protocols for Adult Stem Cells. Methods in Molecular Biology™, vol 621. Humana Press. https://doi.org/10.1007/978-1-60761-063-2_11
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DOI: https://doi.org/10.1007/978-1-60761-063-2_11
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