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. 2014 Oct 14;9(10):e108468. doi: 10.1371/journal.pone.0108468

Figure 6. Rps6kb1 was determined as the direct and functional target of mir-223-3p.

Figure 6

A. The Venn diagram displayed the overlap between three databases. B. Western blot analyzed the protein level of Rps6kb1 in ICM, ICP and ICTF when compared to that of NCM, NCP and NCTF. β-actin was used as internal controls. (C)Real-time PCR analysis showed no significant difference in RPS6KB1 mRNA expression in ICM, ICP and ICTF when compared to that of NCM, NCP and NCTF. *P<0.05, **P<0.01.