Figure 1
Figure 1. Identification of CD19−CD11c−CD35+B220+ cells in mouse spleen. (A) Flow cytometric analysis of spleen cells from C57BL/6J-Jcl mice and TNF-KO mice. Whole spleen cells stained with indicated mAbs were analyzed. Gating of CD19− and CD11c− cells enabled the identification of CD35+ cells in both strains. Frequencies of CD35+B220+ cells within CD19− and CD11c− populations of splenocytes are shown at the corner of respective quadrants. (B) Isolated CD35+B220+ cells show the MHC class II+ phenotype. The phenotype of the isolated cell population, termed CD35+B220+ cells, was characterized by double color staining for MHC class II and CD35. Data are representative of 3 independent experiments. (C) Morphology of CD35+B220+ cells. Isolated CD35+B220+ cells from GFP-Tg mice were added dropwise onto a glass slide, air-dried, and fixed with 4% buffered paraformaldehyde. GFP-mediated signals were observed and photographed with a Leica confocal microscope. Photographs were taken with a 63×/1.4 NA objective.

Identification of CD19CD11cCD35+B220+ cells in mouse spleen. (A) Flow cytometric analysis of spleen cells from C57BL/6J-Jcl mice and TNF-KO mice. Whole spleen cells stained with indicated mAbs were analyzed. Gating of CD19 and CD11c cells enabled the identification of CD35+ cells in both strains. Frequencies of CD35+B220+ cells within CD19 and CD11c populations of splenocytes are shown at the corner of respective quadrants. (B) Isolated CD35+B220+ cells show the MHC class II+ phenotype. The phenotype of the isolated cell population, termed CD35+B220+ cells, was characterized by double color staining for MHC class II and CD35. Data are representative of 3 independent experiments. (C) Morphology of CD35+B220+ cells. Isolated CD35+B220+ cells from GFP-Tg mice were added dropwise onto a glass slide, air-dried, and fixed with 4% buffered paraformaldehyde. GFP-mediated signals were observed and photographed with a Leica confocal microscope. Photographs were taken with a 63×/1.4 NA objective.

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