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Two-color flow cytometric analysis of CD206 expression on mouse peritoneal exudate cells. Thioglycollate-elicited BALB/c mouse peritoneal exudate cells (PEC) were fixed and permeabilized using the BD Pharmingen™ Transcription Factor Buffer Set (Cat. No. 562574/562725). The leucocytes were then stained with PE Rat Anti-Mouse CD107b (Mac-3) antibody (Cat. No. 553324) and either Alexa Fluor® 647 Rat IgG2a, κ Isotype Control (Cat. No. 565250; Left Panel) or Alexa Fluor® 647 Rat Anti-Mouse CD206 antibody (Cat. No. 565250; Right Panel). Two-color flow cytometric contour plots showing the correlated expression of CD206 (or Ig Isotype control staining) versus CD107b were derived from gated events with the forward and side-light scattering characteristics of intact PEC. Flow cytometric analysis was performed using a BD FACSCanto™ II Flow Cytometer System.
Flow cytometric analysis of CD206 expression by J774A cells. Cells from the J774A (Mouse macrophage, ATCC TIB-67) cell line were similarly fixed and permeabilized, stained with either Alexa Fluor® 647 Rat IgG2a, κ Isotype Control (dashed line histogram) or Alexa Fluor® 647 Rat Anti-Mouse CD206 antibody (solid line histogram), and analzyed by flow cytometry. The fluorescence histogram showing CD206 expression (or Ig Isotype control staining) was derived from gated events with the forward and side light-scatter characteristics of intact J774A cells.