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. Author manuscript; available in PMC: 2020 May 1.
Published in final edited form as: J Allergy Clin Immunol. 2018 Nov 12;143(5):1865–1877.e4. doi: 10.1016/j.jaci.2018.08.053

FIG 6. CRF2−/− BMMCs exhibit heightened intracellular Ca2+ store release and expression of SOCE channels.

FIG 6.

BMMCs derived from WT and CRF2−/− mice were loaded with Fluo 4, and intracellular Ca2+ levels were measured following stimulation with IgE/DNP. A,B: Representative intracellular Ca2+ traces for experiments conducted under Ca2+-replete (A) or Ca2+-free (1 mM EDTA; B) conditions. C: Mean peak change in fluorescence following IgE/DNP stimulus presented as ∆ peak fluorescence. D-I: Representative Western blots and densitometry analysis for STIM1 (D, G), TRPC1 (E, H), and Orai (F, I) in WT and CRF2−/− BMMCs. *Significance between groups was determined by an unpaired two-tailed t-test (C, G-I),*p<0.05, **p<0.01.