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Flow cytometric analysis of CD45 expression on mouse splenocytes. Mouse splenic leucocytes were stained with either FITC Rat IgG2b, κ Isotype Control (Cat. No. 553988; dashed line histogram) or FITC Rat Anti-Mouse CD45 antibody (Cat. No. 553079/ 561088/ 553080; solid line histogram) at 0.15 µg/test. The fluorescence histogram showing CD45 fluorescence (or Ig Isotype control staining) was derived from gated events with the forward and side light-scatter characteristics of intact splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa™ Cell Analyzer System X-20 and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
Flow cytometric analysis of CD45 expression on mouse splenocytes. Mouse splenic leucocytes were stained with either FITC Rat IgG2b, κ Isotype Control (Cat. No. 553988; dashed line histogram) or FITC Rat Anti-Mouse CD45 antibody (Cat. No. 553079/ 561088/ 553080; solid line histogram) at 0.15 µg/test. The fluorescence histogram showing CD45 fluorescence (or Ig Isotype control staining) was derived from gated events with the forward and side light-scatter characteristics of intact splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa™ Cell Analyzer System X-20 and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
Flow cytometric analysis of CD45 expression on mouse splenocytes. Mouse splenic leucocytes were stained with either FITC Rat IgG2b, κ Isotype Control (Cat. No. 553988; dashed line histogram) or FITC Rat Anti-Mouse CD45 antibody (Cat. No. 553079/ 561088/ 553080; solid line histogram) at 0.15 µg/test. The fluorescence histogram showing CD45 fluorescence (or Ig Isotype control staining) was derived from gated events with the forward and side light-scatter characteristics of intact splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa™ Cell Analyzer System X-20 and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
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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 cells and BD CompBeads to ensure that BD® CompBeads are appropriate for your specific cellular application.
The 30-F11 clone has been reported to react with all isoforms and both alloantigens of CD45, which is found on hematopoietic stem cells and all cells of hematopoietic origin, except erythrocytes. CD45 is a transmembrane glycoprotein which is expressed at high levels on the cell surface, and its presence distinguishes leukocytes from non-hematopoietic cells. CD45 is a member of the Protein Tyrosine Phosphatase (PTP) family, where the intracellular carboxy-terminal region contains two PTP catalytic domains, and the extracellular region is highly variable due to alternative splicing of exons 4, 5, and 6 (designated as A, B, and C, respectively). CD45 isoforms play complex roles in T-cell and B-cell antigen receptor signal transduction and the CD45 isoforms detected in the mouse are cell type-, maturation-, and activation state-specific.
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