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=1724253058&Signature=LLK0-AUGklfvIOJeaY8c5lTQSor0pK3z7ugaSA-~HIg7yYzBwrgkpasmG0-1DP6cFotvvRJ6P9SvCP9cHw05ZVWTLhC6yMABt5tiQSpPpJXfsWf85REEoXnT1NuXMNzNk0NW8udVSKXu6-8yDxvS1cgRmC1GqREa6jE2lPLloyIHmqRWm1tCuNgsF9opK7pw52mOjwugLQcKTq5Ul3Gnkk7ol6h4ePrDHDIkzPJPK7BhmLAragdT-JKuM5vAAF5AO40XPLTnrXTPNtcqfm7GJ2AWV3mertRBUW7TVG4OD5B496rVfxzyjWOfvQnTF0oG2~qoPwvYXUBxXAv5qySU9g__&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.
