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. Author manuscript; available in PMC: 2011 Jan 15.
Published in final edited form as: J Immunol. 2009 Dec 14;184(2):877–885. doi: 10.4049/jimmunol.0902346

Figure 4. Cell type specific expression of the MIIG transgene and responsiveness to IFN-γ in non-macrophage lineage cells from WT and MIIG mice.

Figure 4

A. Dots plots illustrating how each population is defined by flow cytometry. B. Surface myc staining of indicated populations. C. Phospho-STAT1 staining of the indicated population after in vitro stimulation with IFN-γ. Shaded area represents isotype staining (in B) or fluorescence intensity of phospho-STAT1 in unstimulated cells (in C). D. Expression of the MIIG transgene and β-actin in indicated tissues, as measured by RT PCR of cDNA. Non-hematopoietic tissues were first depleted of CD45+ cells before extraction of RNA, in order to avoid contamination by macrophages. Data are representative of three or more experiments examining greater than 6 mice.

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