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. 2017 Jan 25;6(1):50–60. doi: 10.7774/cevr.2017.6.1.50

Fig. 3. Effects of Src homology 2 domain–containing adaptor protein B (SHB)–knockdown (SHBKD) on bone marrow–derived dendritic cells (BMDC) phenotypes. Dendritic cell (DC) precursor cells were transfected with SHB-specific siRNA (si-shb) or control siRNA (si-con) on day 4 during BMDC development. Cells were harvested 48 hours after transfection and were used as a source of wild type (WT) and SHBKD DCs. (A) Silencing was assessed by Western blot. (B) Representative fluorescence-activated cell sorting data of surface phenotypes showing SHBKD DCs (si-shb) or WT DCs (si-con) in their immature form. (C) Statistical data showing mean fluorescence intensity (MFI) of DC surface phenotypes in B are presented as the mean ± standard deviation from three individual experiments. Student's t test, **p < 0.01, ***p < 0.001 in comparison with WT DCs.

Fig. 3