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Human EDTA-treated whole blood samples were stained with CD21 antibodies as well as CD19 antibodies using a lyse-wash procedure and analyzed by flow cytometry using the MACSQuant ® Analyzer. For analysis, lymphocytes were gated based on forward and side scatter signals and after exclusion of cell debris and red blood cells based on scatter signals and CD45 fluorescence. |
CD21 antibodiesFigure 1Human EDTA-treated whole blood samples were stained with CD21 antibodies as well as CD19 antibodies using a lyse-wash procedure and analyzed by flow cytometry using the MACSQuant ® Analyzer. For analysis, lymphocytes were gated based on forward and side scatter signals and after exclusion of cell debris and red blood cells based on scatter signals and CD45 fluorescence. | CD21 antibodiesFigure 1Human EDTA-treated whole blood samples were stained with CD21 antibodies as well as CD19 antibodies using a lyse-wash procedure and analyzed by flow cytometry using the MACSQuant ® Analyzer. For analysis, lymphocytes were gated based on forward and side scatter signals and after exclusion of cell debris and red blood cells based on scatter signals and CD45 fluorescence. |
Clone | HB5 |
---|---|
Isotype | mouse IgG2a |
Type of antibody | Primary antibodies |
Species | human |
Antigen | CD21 |
Alternative names of antigen | Complement Receptor 2 (CR2), Complement 3d Receptor |
Distribution of antigen | B cells, dendritic cells, T cells |
Human EDTA-treated whole blood samples were stained with CD21 antibodies as well as CD19 antibodies using a lyse-wash procedure and analyzed by flow cytometry using the MACSQuant ® Analyzer. For analysis, lymphocytes were gated based on forward and side scatter signals and after exclusion of cell debris and red blood cells based on scatter signals and CD45 fluorescence. |
CD21 antibodiesFigure 1Human EDTA-treated whole blood samples were stained with CD21 antibodies as well as CD19 antibodies using a lyse-wash procedure and analyzed by flow cytometry using the MACSQuant ® Analyzer. For analysis, lymphocytes were gated based on forward and side scatter signals and after exclusion of cell debris and red blood cells based on scatter signals and CD45 fluorescence. | CD21 antibodiesFigure 1Human EDTA-treated whole blood samples were stained with CD21 antibodies as well as CD19 antibodies using a lyse-wash procedure and analyzed by flow cytometry using the MACSQuant ® Analyzer. For analysis, lymphocytes were gated based on forward and side scatter signals and after exclusion of cell debris and red blood cells based on scatter signals and CD45 fluorescence. |
Clone | HB5 |
---|---|
Isotype | mouse IgG2a |
Type of antibody | Primary antibodies |
Species | human |
Antigen | CD21 |
Alternative names of antigen | Complement Receptor 2 (CR2), Complement 3d Receptor |
Distribution of antigen | B cells, dendritic cells, T cells |
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