BD PharmingenTM Alexa Fluor 647 Rat anti-Mouse CD267

Description

Flow cytometric analysis of Alexa Fluor 647-conjugated anti-Mouse CD267 on mouse spelenocytes. Unstimulated mouse splenocytes were pre-incubated with Mouse BD Fc Block purified anti-mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC-conjugqted anti-mouse CD19 Cat. No. 553785 and Alexa Fluor 647-conjugated anti-mouse CD267 antibody Clone 8F10, Cat. No. 558453; right panel or Alexa Fluor -conjugated rat IgG2a Clone R35-95, Cat. No. 557690; left panel . Flow cytometry was performed and the dot plots were derived from the gated events based on light scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACSCalibur flow cytometry system. Flow cytometric analysis of Alexa Fluor 647-conjugated anti-Mouse CD267 on mouse spelenocytes. Unstimulated mouse splenocytes were pre-incubated with Mouse BD Fc Block purified anti-mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC-conjugqted anti-mouse CD19 Cat. No. 553785 and Alexa Fluor 647-conjugated anti-mouse CD267 antibody Clone 8F10, Cat. No. 558453; right panel or Alexa Fluor -conjugated rat IgG2a Clone R35-95, Cat. No. 557690; left panel . Flow cytometry was performed and the dot plots were derived from the gated events based on light scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACSCalibur flow cytometry system. Flow cytometric analysis of Alexa Fluor 647-conjugated anti-Mouse CD267 on mouse spelenocytes. Unstimulated mouse splenocytes were pre-incubated with Mouse BD Fc Block purified anti-mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC-conjugqted anti-mouse CD19 Cat. No. 553785 and Alexa Fluor 647-conjugated anti-mouse CD267 antibody Clone 8F10, Cat. No. 558453; right panel or Alexa Fluor -conjugated rat IgG2a Clone R35-95, Cat. No. 557690; left panel . Flow cytometry was performed and the dot plots were derived from the gated events based on light scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACSCalibur flow cytometry system. Show More Flow cytometric analysis of Alexa Fluor 647-conjugated anti-Mouse CD267 on mouse spelenocytes. Unstimulated mouse splenocytes were pre-incubated with Mouse BD Fc Block purified anti-mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC-conjugqted anti-mouse CD19 Cat. No. 553785 and Alexa Fluor 647-conjugated anti-mouse CD267 antibody Clone 8F10, Cat. No. 558453; right panel or Alexa Fluor -conjugated rat IgG2a Clone R35-95, Cat. No. 557690; left panel . Flow cytometry was performed and the dot plots were derived from the gated events based on light scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACSCalibur flow cytometry system. Show More Flow cytometric analysis of Alexa Fluor 647-conjugated anti-Mouse CD267 on mouse spelenocytes. Unstimulated mouse splenocytes were pre-incubated with Mouse BD Fc Block purified anti-mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC-conjugqted anti-mouse CD19 Cat. No. 553785 and Alexa Fluor 647-conjugated anti-mouse CD267 antibody Clone 8F10, Cat. No. 558453; right panel or Alexa Fluor -conjugated rat IgG2a Clone R35-95, Cat. No. 557690; left panel . Flow cytometry was performed and the dot plots were derived from the gated events based on light scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACSCalibur flow cytometry system. Flow cytometric analysis of Alexa Fluor 647-conjugated anti-Mouse CD267 on mouse spelenocytes. Unstimulated mouse splenocytes were pre-incubated with Mouse BD Fc Block purified anti-mouse CD16/CD32 mAb 2.4G2 Cat. No. 553141/553142 . The cells were then stained with FITC-conjugqted anti-mouse CD19 Cat. No. 553785 and Alexa Fluor 647-conjugated anti-mouse CD267 antibody Clone 8F10, Cat. No. 558453; right panel or Alexa Fluor -conjugated rat IgG2a Clone R35-95, Cat. No. 557690; left panel . Flow cytometry was performed and the dot plots were derived from the gated events based on light scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACSCalibur flow cytometry system.