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Fig. 2. SkMSCs competently proliferate on the MBP-FGF2-immobilized matrix. (A) Phase-contrast microscopic images of proliferating SkMSCs cultured on Matrigel or MBP-FGF2 matrix-coated surface with or without FGF2 supplementation in the growth medium for 4 days. Scale bar, 50 μm. (B, C) Determination of live SkMSC density with a modified MTS assay. The MTS assay was performed daily during the time course of 4 days. SkMSCs were cultured on BSA-, MBP-FGF2-, or Matrigel-coated 96-well plates in the absence (B) or presence (C) of soluble FGF2 (5 ng/mL) as indicated. Viable cell density was determined from the optical density (O.D.) at 450 nm wavelength. Experiments were performed in triplicates. Data represent normalized mean values with SEM.
International Journal of Stem Cells 2019;12:360-6 https://doi.org/10.15283/ijsc18125
© 2019 International Journal of Stem Cells