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. 2015 Jun 3;10(6):e0127467. doi: 10.1371/journal.pone.0127467

Fig 1.

Fig 1

A. Western blotting using anti-Pin1 antibody and anti- ß-actin antibody as internal controls. LNCap and DU145 cells are transduced with control-siRNA or Pin1 siRNA for 48hr. B. Quantification of bands in Fig 1A. Bars indicate means±S.E. for the ratio of the band intensity of Pin1 to that of ß-actin.