Ides of IRP2 (grey) at their C-termini. (B and C) H1299 cells engineered to express these constructs (in two independent clones) were treated overnight (14 h) with the indicated concentrations of FAC and lysates were subjected to Western blotting with luciferase (top) and β-actin (bottom) antibodies.<p><b>Copyright information:</b></p><p>Taken from "Iron-dependent degradation of IRP2 requires its C-terminal region and IRP structural integrity"</p><p>http://www.biomedcentral.com/1471-2199/9/15</p><p>BMC Molecular Biology 2008;9():15-15.</p><p>Published online 28 Jan 2008</p><p>PMCID:PMC2267205.</p><p></p
