BD Pharmingen- PE Mouse anti-Human CD39_BD Pharmingen
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Flow cytometric analysis of PE Mouse anti-Human CD39 on peripheral blood. Human peripheral blood was isolated by Ficoll gradient and stained simultaneously with PerCP CD4 (clone SK3, Cat. No. 340671), Alexa Fluor 647 CD127 (clone hIL7R-M21, Cat. No. 558598) and PE CD39 (clone TU66, Cat. No. 555464). The cells were then fixed and permeabilized using the Foxp3 buffer kit (Cat. No. 560098) and then stained with Alexa Fluor 488 Foxp3 (clone 259D, Cat. No. 560047).The dot plot (data not shown) was derived from gated events based on light scattering characteristics of lymphocytes and fluorescence characteristics of CD4 positive cells. Regulatory T cells were then identified by the CD127 versus Foxp3 staining pattern (right panel) and analyzed for CD39 expression (left panel). Flow cytometry was performed on a BD FACSCanto™ System.
Flow cytometric analysis of PE Mouse anti-Human CD39 on peripheral blood. Human peripheral blood was isolated by Ficoll gradient and stained simultaneously with PerCP CD4 (clone SK3, Cat. No. 340671), Alexa Fluor 647 CD127 (clone hIL7R-M21, Cat. No. 558598) and PE CD39 (clone TU66, Cat. No. 555464). The cells were then fixed and permeabilized using the Foxp3 buffer kit (Cat. No. 560098) and then stained with Alexa Fluor 488 Foxp3 (clone 259D, Cat. No. 560047).The dot plot (data not shown) was derived from gated events based on light scattering characteristics of lymphocytes and fluorescence characteristics of CD4 positive cells. Regulatory T cells were then identified by the CD127 versus Foxp3 staining pattern (right panel) and analyzed for CD39 expression (left panel). Flow cytometry was performed on a BD FACSCanto™ System.
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