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Multiparameter flow cytometric analysis of CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either FITC Mouse IgG2a, κ Isotype Control (Cat. No. 553456; Left Plot) or FITC Mouse Anti-Human CD3 antibody (Cat. No. 566783; Right Plot). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-parameter pseudocolor dot plot showing the correlated expression of CD3 (or Ig Isotype control staining) versus side light-scatter (SSC) signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD Celesta™ Cell Analyzer System and FlowJo™ software.
Multiparameter flow cytometric analysis of CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either FITC Mouse IgG2a, κ Isotype Control (Cat. No. 553456; Left Plot) or FITC Mouse Anti-Human CD3 antibody (Cat. No. 566783; Right Plot). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-parameter pseudocolor dot plot showing the correlated expression of CD3 (or Ig Isotype control staining) versus side light-scatter (SSC) signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD Celesta™ Cell Analyzer System and FlowJo™ software.
Multiparameter flow cytometric analysis of CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either FITC Mouse IgG2a, κ Isotype Control (Cat. No. 553456; Left Plot) or FITC Mouse Anti-Human CD3 antibody (Cat. No. 566783; Right Plot). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-parameter pseudocolor dot plot showing the correlated expression of CD3 (or Ig Isotype control staining) versus side light-scatter (SSC) signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD Celesta™ Cell Analyzer System and FlowJo™ software.
Multiparameter flow cytometric analysis of CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either FITC Mouse IgG2a, κ Isotype Control (Cat. No. 553456; Left Plot) or FITC Mouse Anti-Human CD3 antibody (Cat. No. 566783; Right Plot). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-parameter pseudocolor dot plot showing the correlated expression of CD3 (or Ig Isotype control staining) versus side light-scatter (SSC) signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD Celesta™ Cell Analyzer System and FlowJo™ software.
Multiparameter flow cytometric analysis of CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either FITC Mouse IgG2a, κ Isotype Control (Cat. No. 553456; Left Plot) or FITC Mouse Anti-Human CD3 antibody (Cat. No. 566783; Right Plot). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-parameter pseudocolor dot plot showing the correlated expression of CD3 (or Ig Isotype control staining) versus side light-scatter (SSC) signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD Celesta™ Cell Analyzer System and FlowJo™ software.
Multiparameter flow cytometric analysis of CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either FITC Mouse IgG2a, κ Isotype Control (Cat. No. 553456; Left Plot) or FITC Mouse Anti-Human CD3 antibody (Cat. No. 566783; Right Plot). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The two-parameter pseudocolor dot plot showing the correlated expression of CD3 (or Ig Isotype control staining) versus side light-scatter (SSC) signals was derived from gated events with the forward and side light-scatter characteristics of viable leucocyte populations. Flow cytometry and data analysis were performed using a BD Celesta™ Cell Analyzer System and FlowJo™ software.
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BD® CompBeads can be used as surrogates to assess fluorescence spillover (compensation). When fluorochrome conjugated antibodies are bound to BD® CompBeads, they have spectral properties very similar to cells. However, for some fluorochromes there can be small differences in spectral emissions compared to cells, resulting in spillover values that differ when compared to biological controls. It is strongly recommended that when using a reagent for the first time, users compare the spillover on cell and BD® CompBeads to ensure that BD® CompBeads are appropriate for your specific cellular application.
The OKT3 monoclonal antibody specifically recognizes the CD3 epsilon subunit (CD3e/CD3ε) of the CD3 complex which consists of four transmembrane proteins (γ, δ, ε, ζ) that are associated with the T cell antigen receptor (TCR) to form the CD3/TCR complex. The CD3 complex associates with either TCR αβ or TCR γδ heterodimers that are alternatively expressed by some thymocytes, T cells or NKT cells. The CD3 complex is required for the cell surface expression and signal-transducing functions of the TCR. The CD3 complex is expressed by ~60-85% thymocytes and by all peripheral mature T cells. CD3e is also known as T3E or TCRE. CD3e is a ~20 kDa unglycosylated type I transmembrane protein that is encoded by CD3E which belongs to the immunoglobulin superfamily (IgSF). CD3e has an Ig-like extracellular domain (ECD) and an immunoreceptor tyrosine-based activation motif (ITAM) in its cytoplasmic domain. The OKT3 antibody can reportedly fix complement, stimulate T cell proliferation and cytokine production, and block the binding of other human CD3e-specific antibodies including UCHT1 and SK7.
Fluorescein (FITC) is part of the BD blue family of dyes. This is a small organic fluorochrome with an excitation maximum (Ex Max) at 494-nm and an emission maximum (Em Max) at 518-nm. FITC is designed to be excited by the Blue laser (488-nm) and detected using an optical filter centered near 520 nm (e.g., a 530/30-nm bandpass filter). Please ensure that your instrument's configurations (lasers and optical filters) are appropriate for this dye.
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