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Objectives: Human pluripotent stem cell derived cardiomyocytes (hPSC-CMs) are highly heterogeneous and show a variety of chamber types (ventricular, atrial and pacemaker) and maturation states.Immunophenotyping and isolation of homogeneous subpopulations using antibodies against surface proteins would be critical for the use of hPSC-CMs for drug screening and transplantation.Our aim is to characterize the suffaceome of hPSC-CMs.