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. Author manuscript; available in PMC: 2008 Mar 30.
Published in final edited form as: Biochem Biophys Res Commun. 2007 Feb 2;355(1):217–220. doi: 10.1016/j.bbrc.2007.01.136

Fig. 1.

Fig. 1

Cytosolic (A) or nuclear (B) protein extracts and radiolabeled probes corresponding to the C/EBPβ 5′-UTR and coding regions (lanes 1–9 as detailed in Methods) were used to perform RNA gel shift and supershift assays (Ab, anti-HuR monoclonal antibody). A radiolabeled probe corresponding to a section of the C/EBPβ 3′-UTR previously demonstrated to bind HuR [1] was included as a positive control, (lanes 10–12).