Fig. 4.
![Fig. 4. Induction kinetics of IRPs by Epo in MEL cells. Cells were treated for 24 hours with 50 μmol/L Fe(NO3 )3 (I), with 100 μmol/L desferrioxamine (D), and, for the indicated times, with murine recombinant Epo (0.5 U/mL) or remained untreated (control [C]). Gel retardation assays were performed exactly as described in the legend to Fig 1. The results of one of three representative experiments are shown.](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/89/2/10.1182_blood.v89.2.680/4/bl_0026f4.jpeg?Expires=1735843569&Signature=pnb5lXuF~8GpPcybBc-UVe9mrJldAsa6LRVH~cT4UngqOkme~2FkjAPmKmKjIyNtNlIMk4EaWZ6FVf-2C4cH-YT4aANptNa~BXAdnMszeabRoEtnxQXrns4fuDnHUGmmX~GiNbnNmZbi2Z-TfjcfiF5b5iBZ3ggclSkBn~iNI4LHYKZC2klKsEerWXbDl9HMGw1e0lVHCexOo~-WW9jlNLfY~o0XC5whSAIAGfwc900Cp-PNYYvMYIGfnT9fuy5ZlIKE~qQY8gfH7LnJXmmTVlYry5CbeqJshYVjQV3upPjhCWjLgG90LBlet4r7Jx8nmzYRe2a1xKijhHMfJKNdHQ__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)
Induction kinetics of IRPs by Epo in MEL cells. Cells were treated for 24 hours with 50 μmol/L Fe(NO3 )3 (I), with 100 μmol/L desferrioxamine (D), and, for the indicated times, with murine recombinant Epo (0.5 U/mL) or remained untreated (control [C]). Gel retardation assays were performed exactly as described in the legend to Fig 1. The results of one of three representative experiments are shown.
