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. 2023 Jun 28;25(6):372–382. doi: 10.22074/CELLJ.2023.563370.1148

Fig.1.

Fig.1

Decellularization procedure, hydrogel formation and characterization. A. Schematic representation of lung decellularization procedure and hydrogel formation, B. Histological analysis of native sheep lung and decellularized sheep lung ECM-derived scaffold using H&E, Alcian blue, MT, Toluidine blue and DAPI staining (n=3 biological repeats, scale bar: 50 µm), C. Representative SEM photomicrographs of native lung (scale bar: 200 µm) and decellularized lung ECM-derived scaffold (scale bar: 50 µm). D. Quantification of GAGs content of native and decellularized scaffold (n=4). E. DNA quantification assay (n=3). DDW; Double distilled water, SDC; Sodium deoxycholate, PBS; Phosphate buffered saline, MT; Masson’s trichrome, SEM; scanning electron microscopy, ECM; Extracellular matrix, GAGs; glycosaminoglycans, h; Hour, ns; Not significant, and ***; P<0.001.