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BD PharmingenTM PE Rat Anti-Human CD115 (CSF-1R)

565368 ·

BDB Bioscience · Cat: 565368

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Catalog No: 565368
Category: reagents
Brand: BDB Bioscience

Description

Multiparameter flow cytometric analysis of CD115 CSF-1R expression on human peripheral blood leucocytes. Whole blood cells were stained with either PE Rat IgG1, kappa Isotype Control Cat. No. 553925; left panel or PE Rat Anti-Human CD115 CSF-1R Cat. No. 565368; right panel . The erythrocytes were lysed with Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric contour plots showing the correlated expression of CD115 CSF-1R or Ig Isotype control staining versus Side Light Scatter SSC-A signals were derived from gated events with the forward and side light-scattering characteristics of viable leucocytes. Flow cytometric analysis was performed on a BD LSR II. Multiparameter flow cytometric analysis of CD115 CSF-1R expression on human peripheral blood leucocytes. Whole blood cells were stained with either PE Rat IgG1, kappa Isotype Control Cat. No. 553925; left panel or PE Rat Anti-Human CD115 CSF-1R Cat. No. 565368; right panel . The erythrocytes were lysed with Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric contour plots showing the correlated expression of CD115 CSF-1R or Ig Isotype control staining versus Side Light Scatter SSC-A signals were derived from gated events with the forward and side light-scattering characteristics of viable leucocytes. Flow cytometric analysis was performed on a BD LSR II. Multiparameter flow cytometric analysis of CD115 CSF-1R expression on human peripheral blood leucocytes. Whole blood cells were stained with either PE Rat IgG1, kappa Isotype Control Cat. No. 553925; left panel or PE Rat Anti-Human CD115 CSF-1R Cat. No. 565368; right panel . The erythrocytes were lysed with Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric contour plots showing the correlated expression of CD115 CSF-1R or Ig Isotype control staining versus Side Light Scatter SSC-A signals were derived from gated events with the forward and side light-scattering characteristics of viable leucocytes. Flow cytometric analysis was performed on a BD LSR II. Show More Multiparameter flow cytometric analysis of CD115 CSF-1R expression on human peripheral blood leucocytes. Whole blood cells were stained with either PE Rat IgG1, kappa Isotype Control Cat. No. 553925; left panel or PE Rat Anti-Human CD115 CSF-1R Cat. No. 565368; right panel . The erythrocytes were lysed with Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric contour plots showing the correlated expression of CD115 CSF-1R or Ig Isotype control staining versus Side Light Scatter SSC-A signals were derived from gated events with the forward and side light-scattering characteristics of viable leucocytes. Flow cytometric analysis was performed on a BD LSR II. Show More Multiparameter flow cytometric analysis of CD115 CSF-1R expression on human peripheral blood leucocytes. Whole blood cells were stained with either PE Rat IgG1, kappa Isotype Control Cat. No. 553925; left panel or PE Rat Anti-Human CD115 CSF-1R Cat. No. 565368; right panel . The erythrocytes were lysed with Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric contour plots showing the correlated expression of CD115 CSF-1R or Ig Isotype control staining versus Side Light Scatter SSC-A signals were derived from gated events with the forward and side light-scattering characteristics of viable leucocytes. Flow cytometric analysis was performed on a BD LSR II. Multiparameter flow cytometric analysis of CD115 CSF-1R expression on human peripheral blood leucocytes. Whole blood cells were stained with either PE Rat IgG1, kappa Isotype Control Cat. No. 553925; left panel or PE Rat Anti-Human CD115 CSF-1R Cat. No. 565368; right panel . The erythrocytes were lysed with Lysing Buffer Cat. No. 555899 . Two-parameter flow cytometric contour plots showing the correlated expression of CD115 CSF-1R or Ig Isotype control staining versus Side Light Scatter SSC-A signals were derived from gated events with the forward and side light-scattering characteristics of viable leucocytes. Flow cytometric analysis was performed on a BD LSR II.

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