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Multiparameter flow cytometric analysis of CD11b expression on rat bone marrow. Lewis rat bone marrow cells were stained with either BD Horizon™ V450 Mouse IgA, κ Isotype Control (Cat. No. 562142, Left Panel) or a BD Horizon™ V450 Mouse Anti-Rat CD11b antibody (Cat. No. 562108, Right Panel). Two parameter flow cytometric dot blots showing side light scatter signals (SSC-A) versus CD11b expression (or Ig Isotype Control staining) were derived from gated events with the forward light-scatter characteristics of viable bone marrow cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Multiparameter flow cytometric analysis of CD11b expression on rat bone marrow. Lewis rat bone marrow cells were stained with either BD Horizon™ V450 Mouse IgA, κ Isotype Control (Cat. No. 562142, Left Panel) or a BD Horizon™ V450 Mouse Anti-Rat CD11b antibody (Cat. No. 562108, Right Panel). Two parameter flow cytometric dot blots showing side light scatter signals (SSC-A) versus CD11b expression (or Ig Isotype Control staining) were derived from gated events with the forward light-scatter characteristics of viable bone marrow cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Multiparameter flow cytometric analysis of CD11b expression on rat bone marrow. Lewis rat bone marrow cells were stained with either BD Horizon™ V450 Mouse IgA, κ Isotype Control (Cat. No. 562142, Left Panel) or a BD Horizon™ V450 Mouse Anti-Rat CD11b antibody (Cat. No. 562108, Right Panel). Two parameter flow cytometric dot blots showing side light scatter signals (SSC-A) versus CD11b expression (or Ig Isotype Control staining) were derived from gated events with the forward light-scatter characteristics of viable bone marrow cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Multiparameter flow cytometric analysis of CD11b expression on rat bone marrow. Lewis rat bone marrow cells were stained with either BD Horizon™ V450 Mouse IgA, κ Isotype Control (Cat. No. 562142, Left Panel) or a BD Horizon™ V450 Mouse Anti-Rat CD11b antibody (Cat. No. 562108, Right Panel). Two parameter flow cytometric dot blots showing side light scatter signals (SSC-A) versus CD11b expression (or Ig Isotype Control staining) were derived from gated events with the forward light-scatter characteristics of viable bone marrow cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Multiparameter flow cytometric analysis of CD11b expression on rat bone marrow. Lewis rat bone marrow cells were stained with either BD Horizon™ V450 Mouse IgA, κ Isotype Control (Cat. No. 562142, Left Panel) or a BD Horizon™ V450 Mouse Anti-Rat CD11b antibody (Cat. No. 562108, Right Panel). Two parameter flow cytometric dot blots showing side light scatter signals (SSC-A) versus CD11b expression (or Ig Isotype Control staining) were derived from gated events with the forward light-scatter characteristics of viable bone marrow cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Multiparameter flow cytometric analysis of CD11b expression on rat bone marrow. Lewis rat bone marrow cells were stained with either BD Horizon™ V450 Mouse IgA, κ Isotype Control (Cat. No. 562142, Left Panel) or a BD Horizon™ V450 Mouse Anti-Rat CD11b antibody (Cat. No. 562108, Right Panel). Two parameter flow cytometric dot blots showing side light scatter signals (SSC-A) versus CD11b expression (or Ig Isotype Control staining) were derived from gated events with the forward light-scatter characteristics of viable bone marrow cells. Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
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The WT.5 monoclonal antibody specifically binds to CD11b, the α subunit of Mac-1 found on neutrophils and myeloid cells, but not on lymphocytes. Mac-1 expression is rapidly upregulated on neutrophils after activation, in the same time period that CD62L (L-selectin) is shed from the cell surface. Mac-1 mediates adhesion to ICAM-1 (CD54) and C3bi. Neutrophil binding to ICAM-1 is blocked by mAb WT.5.
The antibody is conjugated to BD Horizon™ V450, which has been developed for use in multicolor flow cytometry experiments and is available exclusively from BD Biosciences. It is excited by the Violet laser Ex max of 406 nm and has an Em Max at 450 nm. Conjugates with BD Horizon™ V450 can be used in place of Pacific Blue™ conjugates.
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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.