BD PharmingenTM Alexa Fluor 647 Mouse anti-Mouse CD64 a and b Alloantigens

Description

Flow cytometric analysis of Alexa Fluor 647 Anti-Mouse CD64 recognizing a and b Alloantigens on mouse bone marrow cells. Isolated murine bone marrow cells were preincubated with Mouse BD Fc Block purified Anti-Mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC Anti-CD11b clone M1/70, Cat. No. 553310 and either Alexa Fluor 647 Anti-CD64 clone X54-5/7.1, Cat. No. 558539, right panel or a Alexa Fluor 647 Mouse IgG1 isotype control Cat. No. 557732, left panel . Flow cytometry was performed on a BD FACSCalibur System and the dot plots were derived from the gated events based on light scattering characteristics of viable bone marrow cells. Flow cytometric analysis of Alexa Fluor 647 Anti-Mouse CD64 recognizing a and b Alloantigens on mouse bone marrow cells. Isolated murine bone marrow cells were preincubated with Mouse BD Fc Block purified Anti-Mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC Anti-CD11b clone M1/70, Cat. No. 553310 and either Alexa Fluor 647 Anti-CD64 clone X54-5/7.1, Cat. No. 558539, right panel or a Alexa Fluor 647 Mouse IgG1 isotype control Cat. No. 557732, left panel . Flow cytometry was performed on a BD FACSCalibur System and the dot plots were derived from the gated events based on light scattering characteristics of viable bone marrow cells. Flow cytometric analysis of Alexa Fluor 647 Anti-Mouse CD64 recognizing a and b Alloantigens on mouse bone marrow cells. Isolated murine bone marrow cells were preincubated with Mouse BD Fc Block purified Anti-Mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC Anti-CD11b clone M1/70, Cat. No. 553310 and either Alexa Fluor 647 Anti-CD64 clone X54-5/7.1, Cat. No. 558539, right panel or a Alexa Fluor 647 Mouse IgG1 isotype control Cat. No. 557732, left panel . Flow cytometry was performed on a BD FACSCalibur System and the dot plots were derived from the gated events based on light scattering characteristics of viable bone marrow cells. Show More Flow cytometric analysis of Alexa Fluor 647 Anti-Mouse CD64 recognizing a and b Alloantigens on mouse bone marrow cells. Isolated murine bone marrow cells were preincubated with Mouse BD Fc Block purified Anti-Mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC Anti-CD11b clone M1/70, Cat. No. 553310 and either Alexa Fluor 647 Anti-CD64 clone X54-5/7.1, Cat. No. 558539, right panel or a Alexa Fluor 647 Mouse IgG1 isotype control Cat. No. 557732, left panel . Flow cytometry was performed on a BD FACSCalibur System and the dot plots were derived from the gated events based on light scattering characteristics of viable bone marrow cells. Show More Flow cytometric analysis of Alexa Fluor 647 Anti-Mouse CD64 recognizing a and b Alloantigens on mouse bone marrow cells. Isolated murine bone marrow cells were preincubated with Mouse BD Fc Block purified Anti-Mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC Anti-CD11b clone M1/70, Cat. No. 553310 and either Alexa Fluor 647 Anti-CD64 clone X54-5/7.1, Cat. No. 558539, right panel or a Alexa Fluor 647 Mouse IgG1 isotype control Cat. No. 557732, left panel . Flow cytometry was performed on a BD FACSCalibur System and the dot plots were derived from the gated events based on light scattering characteristics of viable bone marrow cells. Flow cytometric analysis of Alexa Fluor 647 Anti-Mouse CD64 recognizing a and b Alloantigens on mouse bone marrow cells. Isolated murine bone marrow cells were preincubated with Mouse BD Fc Block purified Anti-Mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC Anti-CD11b clone M1/70, Cat. No. 553310 and either Alexa Fluor 647 Anti-CD64 clone X54-5/7.1, Cat. No. 558539, right panel or a Alexa Fluor 647 Mouse IgG1 isotype control Cat. No. 557732, left panel . Flow cytometry was performed on a BD FACSCalibur System and the dot plots were derived from the gated events based on light scattering characteristics of viable bone marrow cells.