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. Author manuscript; available in PMC: 2012 Jun 1.
Published in final edited form as: Neurobiol Dis. 2011 Feb 3;42(3):292–299. doi: 10.1016/j.nbd.2011.01.019

Figure 3.

Figure 3

Flow cytometry of BMM derived from WT and CD36 −/− mice. BMM (5 × 105 cells/assay) were cultured for 7 days and labeled with fluorescently-conjugated primary antibodies to monocytes/macrophages surface markers as described in Methods. Isotype specific immunoglobulins were used in each sample to demonstrate the specificity of the profile. Results show that CD+/+ and CD36−/− BMM were indistinguishable, considering their expression of specific cell surface markers.