Skip to main content
. 2019 Dec 3;2:450. doi: 10.1038/s42003-019-0698-6

Fig. 2.

Fig. 2

Dap12-dependent cell surface expression of mCD33. a Sequence alignment of the transmembrane segment of three murine Siglecs bearing a transmembrane lysine residue, shown in bold, along with hCD33. b Flow cytometry analysis of mCD33 expression on WT and CRISPR/Cas9-generated Dap12−/− RAW264.7 cells (gray: isotype control; black: αmCD33). c WT and Dap12−/− RAW264.7 cells were transiently transfected with mDap12 (red) or empty vector (black) and stained with αmCD33 (black and red) or isotype (gray). d Expression of mCD33 on WT (black), mCD33−/− (gray), and Dap12−/− (red) peripheral blood neutrophils (CD11b+Ly-6G+Ly-6C). e Expression analysis of Dap12 and hCD33 on WT (black) and Dap12−/− U937 cells (red); isotype is shown in gray and was at the same levels for both cell types.