Figure 7
Figure 7. Expression of Ppef2 and Pftk1 in DCs. (A) Gene expression profiling of ex vivo spleen cells. After density enrichment, DCs were sorted on a BD FACSAria instrument based on their expression of CD11c, MHCII, and CD8. CD8 T cells were identified as CD3+, CD8+, and CD4− cells. Gene expression levels were calculated relative to ubiquitin C. Error bars represent SD between 2 independently performed experiments. (B) Gene expression profiling of DCs generated in vitro. Real-time PCR analysis of RNA from samples isolated at days 0, 4, 7, and 8 during DC culture. At day 7, parts of the cultures were stimulated overnight with LPS (2 μg/mL). Shown is relative gene expression after normalization to ubiquitin C. Data are representative of 2 independently performed experiments. nd indicates not detectable.

Expression of Ppef2 and Pftk1 in DCs. (A) Gene expression profiling of ex vivo spleen cells. After density enrichment, DCs were sorted on a BD FACSAria instrument based on their expression of CD11c, MHCII, and CD8. CD8 T cells were identified as CD3+, CD8+, and CD4 cells. Gene expression levels were calculated relative to ubiquitin C. Error bars represent SD between 2 independently performed experiments. (B) Gene expression profiling of DCs generated in vitro. Real-time PCR analysis of RNA from samples isolated at days 0, 4, 7, and 8 during DC culture. At day 7, parts of the cultures were stimulated overnight with LPS (2 μg/mL). Shown is relative gene expression after normalization to ubiquitin C. Data are representative of 2 independently performed experiments. nd indicates not detectable.

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