Figure 1
From: Assessing fatty acid oxidation flux in rodent cardiomyocyte models
Application of the FAO flux protocol for comparison of cardiomyocyte-types (A) Assay setup; (B) Inverted microscope images of cardiomyocyte-types, 20× magnification; (C) Quantification of FAO flux in neonatal rat cardiomyocytes (nRCM), HL1 cardiomyocytes (HL1), adult rat cardiomyocytes (aRCM) fresh and cultured (n = 4; 3; 17; 3); (D) and (E) Representative western blot and quantification of OXPHOS protein; the full-length blot is presented in Supplementary Figure S1. Data are presented as mean ± SEM; *p < 0.01 vs nRCM, #p < 0.01 vs HL1.
