BD PharmingenTM PE Mouse Anti-Human FcepsilonR1alpha

Description

Two-parameter flow cytometric analysis of FcepsilonR1alpha expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG2b, kappa Isotype Control Cat. No. 555058; Left Plot or PE Mouse Anti-Human FcepsilonR1alpha antibody Cat. No. 566607/566608; Right Plot at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric pseudo color plots showing the correlated expression of FcepsilonR1alpha or Ig Isotype control staining versus side light-scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCelesta Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Two-color flow cytometric analysis of FcepsilonR1alpha expression on human peripheral blood lymphocytes. Human whole blood was stained with APC Mouse Anti-Human CD203c antibody Cat. No. 562973 and either PE Mouse IgG2b, kappa Isotype Control Cat. No. 555058; Left Plot or PE Mouse Anti-Human FcepsilonR1alpha antibody Cat. No. 566607/566608; Right Plot at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric pseudo color plots showing the correlated expression of CD203c versus FcepsilonR1alpha or Ig Isotype control staining were derived from gated events with the light scattering characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD FACSCelesta Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Two-parameter flow cytometric analysis of FcepsilonR1alpha expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG2b, kappa Isotype Control Cat. No. 555058; Left Plot or PE Mouse Anti-Human FcepsilonR1alpha antibody Cat. No. 566607/566608; Right Plot at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric pseudo color plots showing the correlated expression of FcepsilonR1alpha or Ig Isotype control staining versus side light-scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCelesta Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Show More Two-color flow cytometric analysis of FcepsilonR1alpha expression on human peripheral blood lymphocytes. Human whole blood was stained with APC Mouse Anti-Human CD203c antibody Cat. No. 562973 and either PE Mouse IgG2b, kappa Isotype Control Cat. No. 555058; Left Plot or PE Mouse Anti-Human FcepsilonR1alpha antibody Cat. No. 566607/566608; Right Plot at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric pseudo color plots showing the correlated expression of CD203c versus FcepsilonR1alpha or Ig Isotype control staining were derived from gated events with the light scattering characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD FACSCelesta Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Show More Two-parameter flow cytometric analysis of FcepsilonR1alpha expression on human peripheral blood leucocyte populations. Human whole blood was stained with either PE Mouse IgG2b, kappa Isotype Control Cat. No. 555058; Left Plot or PE Mouse Anti-Human FcepsilonR1alpha antibody Cat. No. 566607/566608; Right Plot at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric pseudo color plots showing the correlated expression of FcepsilonR1alpha or Ig Isotype control staining versus side light-scatter signals SSC-A were derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometric analysis was performed using a BD FACSCelesta Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific. Two-color flow cytometric analysis of FcepsilonR1alpha expression on human peripheral blood lymphocytes. Human whole blood was stained with APC Mouse Anti-Human CD203c antibody Cat. No. 562973 and either PE Mouse IgG2b, kappa Isotype Control Cat. No. 555058; Left Plot or PE Mouse Anti-Human FcepsilonR1alpha antibody Cat. No. 566607/566608; Right Plot at 1 mug/test. Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two-color flow cytometric pseudo color plots showing the correlated expression of CD203c versus FcepsilonR1alpha or Ig Isotype control staining were derived from gated events with the light scattering characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD FACSCelesta Flow Cytometer System. Data shown on this Technical Data Sheet are not lot specific.