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. Author manuscript; available in PMC: 2012 Dec 1.
Published in final edited form as: Immunol Res. 2011 Dec;51(2-3):227–236. doi: 10.1007/s12026-011-8249-3

Fig. 5. LPS-induced signaling in RIP1−/− B cells.

Fig. 5

Peripheral B cells purified from NSG recipients transferred with RIP1−/− or RIP1+/+ fetal liver cells (A and B) or MEFs of the indicated genotypes (C) were stimulated with LPS (10 μg/ml), and western blotting analysis was performed using Abs specific for p-p65 NF-κB, p-IκB, IκB, and p-Akt. D, The CD69 and CD86 activation markers on B cells were analyzed by flow cytometry 12 hours post stimulation with LPS (1 μg/ml). Unstimulated B cells were used as a control. Data shown are representative of at least 4 independent experiments.