Skip to main content
. 2017 Mar 22;12(3):e0174381. doi: 10.1371/journal.pone.0174381

Fig 2. MCPIP1-D141N with completely abolished RNase activity retains interaction ability against the 3'UTR of C/EBPβ mRNA.

Fig 2

Results of electrophoretic mobility shift assays performed with increasing amounts (0–200 pmol) of recombinant MCPIP1-D141N A. or PIN domain alone, MCPIP1 PIN-D141N B. incubated with 2 pmol of in vitro–transcribed the 3'UTR fragments of C/EBPβ mRNA.