Human lipoaspirate was processed to remove both cellular and lipid content. Raw lipoaspirate (A,D,G,J) was decellularized for 48 hours in SDS or sodium deoxycholate to produce a lipid filled, acellular matrix (B,E,H,K). Removal of lipids using lipase produced a white ECM, free of cellular and lipid content (C,F,I,L). H&E staining (D,E,F) and Hoechst staining (J,K,L) confirmed the absence of nuclei after processing. Oil red O staining (G,H,I) confirmed the removal of lipids. Scale bars = 100 μm.