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Multicolor flow cytometric analysis of TCR βF1 expression by human peripheral blood lymphocytes. Whole blood was surface stained with FITC Mouse Anti-Human TCR αβ (Cat. No. 555547; Top Plots) and PE Mouse Anti-Human TCR γδ (Cat. No. 561994; Bottom Plots) antibodies. Erythrocytes were lysed and leucocytes were fixed with 1x BD Phosflow™ Lyse/Fix Buffer (Cat. No. 558049). After permeabilization with BD™ Phosflow Perm Buffer I (Cat. No. 557885), the cells were then stained with either APC Mouse IgG1, κ Isotype Control (Cat. No. 554681; Left Plots) or APC Mouse Anti-Human TCR βF1 antibody (Cat. No. 566052; Right Plots). Two color contour plots showing the correlated expression of TCR βF1 (or Ig Isotype control staining) versus TCR αβ or TCR γδ were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Multicolor flow cytometric analysis of TCR βF1 expression by human peripheral blood lymphocytes. Whole blood was surface stained with FITC Mouse Anti-Human TCR αβ (Cat. No. 555547; Top Plots) and PE Mouse Anti-Human TCR γδ (Cat. No. 561994; Bottom Plots) antibodies. Erythrocytes were lysed and leucocytes were fixed with 1x BD Phosflow™ Lyse/Fix Buffer (Cat. No. 558049). After permeabilization with BD™ Phosflow Perm Buffer I (Cat. No. 557885), the cells were then stained with either APC Mouse IgG1, κ Isotype Control (Cat. No. 554681; Left Plots) or APC Mouse Anti-Human TCR βF1 antibody (Cat. No. 566052; Right Plots). Two color contour plots showing the correlated expression of TCR βF1 (or Ig Isotype control staining) versus TCR αβ or TCR γδ were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Multicolor flow cytometric analysis of TCR βF1 expression by human peripheral blood lymphocytes. Whole blood was surface stained with FITC Mouse Anti-Human TCR αβ (Cat. No. 555547; Top Plots) and PE Mouse Anti-Human TCR γδ (Cat. No. 561994; Bottom Plots) antibodies. Erythrocytes were lysed and leucocytes were fixed with 1x BD Phosflow™ Lyse/Fix Buffer (Cat. No. 558049). After permeabilization with BD™ Phosflow Perm Buffer I (Cat. No. 557885), the cells were then stained with either APC Mouse IgG1, κ Isotype Control (Cat. No. 554681; Left Plots) or APC Mouse Anti-Human TCR βF1 antibody (Cat. No. 566052; Right Plots). Two color contour plots showing the correlated expression of TCR βF1 (or Ig Isotype control staining) versus TCR αβ or TCR γδ were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
The 8A3 monoclonal antibody is also known as the β Framework 1 (βF1) antibody. After treatment of lymphoid cells with permeabilization reagents, this antibody recognizes a common epitope on the β chain of the T Cell Receptor (TCR) for antigen which is expressed by thymocytes and peripheral T lymphocytes. It does not react with γδ TCR-bearing T cells. The 8A3 antibody does not stain the surface of living cells. This suggests that the TCR β constant region epitope recognized by the 8A3 antibody is normally hidden on viable cells.
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Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Refer to manufacturer's instructions for use and related User Manuals and Technical Data Sheets before using this product as described.
Comparisons, where applicable, are made against older BD technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.