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. 2018 Mar 15;39(4):569–578. doi: 10.1038/aps.2018.19

Figure 5.

Figure 5

Identification of Rab27a and Rab27b expression in Ctrl, SJP, TMP and BOR treated C-MSCs. (A) Real-time PCR results show Rab27a mRNA expression in Ctrl, SJP, TMP and BOR treated C-MSCs (NS, n=3); (B) Staining of Rab27a in Ctrl and SJP treated C-MSCs; (C, D) Western blot results show protein level of Rab27a in Ctrl, SJP, TMP and BOR treated C-MSCs. Densitometric arbitrary units were normalized to GAPDH abundance and are expressed as the mean ± SEM (*P<0.05 vs Ctrl, TMP & BOR, n=5); (E) Real-time PCR results show Rab27b mRNA expression in Ctrl, SJP, TMP and BOR treated C-MSCs (*P<0.05, n=3); (F) Staining of Rab27b in Ctrl and SJP treated C-MSCs; (G, H) Western blot results show protein level of Rab27b in Ctrl, SJP, TMP and BOR treated C-MSCs. Densitometric arbitrary units were normalized to GAPDH abundance and are expressed as the mean±SEM (*P<0.05, n=5); (I, J) Western blot results show protein level of SYTL4 in Ctrl, SJP, TMP and BOR treated C-MSCs. Densitometric arbitrary units were normalized to GAPDH abundance and are expressed as the mean±SEM (*P<0.05 vs Ctrl, TMP & BOR, n=3).