BD PharmingenTM PE-CyTM7 Rat Anti-Mouse CD86

Description

Flow cytometric analysis of CD86 on mouse splenocytes. Left Panel: LPS-stimulated C57BL/6 splenocytes 72 hr were stained either with a PE-Cy7 Rat IgG2a, kappa isotype control shaded or with the PE-Cy7 Rat Anti-Mouse CD86 antibody unshaded . Right Panel: Freshly isolated unstimulated C57BL/6 splenocytes shaded and LPS-stimulated C57BL/6 splenocytes 72 hr unshaded were stained with the PE-Cy7 Rat Anti-Mouse CD86 antibody. Histograms were derived from gated events based on light scattering characteristics for lymphocytes. Flow cytometry was performed on a BD LSR II flow cytometry system. Flow cytometric analysis of CD86 on mouse splenocytes. Left Panel: LPS-stimulated C57BL/6 splenocytes 72 hr were stained either with a PE-Cy7 Rat IgG2a, kappa isotype control shaded or with the PE-Cy7 Rat Anti-Mouse CD86 antibody unshaded . Right Panel: Freshly isolated unstimulated C57BL/6 splenocytes shaded and LPS-stimulated C57BL/6 splenocytes 72 hr unshaded were stained with the PE-Cy7 Rat Anti-Mouse CD86 antibody. Histograms were derived from gated events based on light scattering characteristics for lymphocytes. Flow cytometry was performed on a BD LSR II flow cytometry system. Flow cytometric analysis of CD86 on mouse splenocytes. Left Panel: LPS-stimulated C57BL/6 splenocytes 72 hr were stained either with a PE-Cy7 Rat IgG2a, kappa isotype control shaded or with the PE-Cy7 Rat Anti-Mouse CD86 antibody unshaded . Right Panel: Freshly isolated unstimulated C57BL/6 splenocytes shaded and LPS-stimulated C57BL/6 splenocytes 72 hr unshaded were stained with the PE-Cy7 Rat Anti-Mouse CD86 antibody. Histograms were derived from gated events based on light scattering characteristics for lymphocytes. Flow cytometry was performed on a BD LSR II flow cytometry system. Show More Flow cytometric analysis of CD86 on mouse splenocytes. Left Panel: LPS-stimulated C57BL/6 splenocytes 72 hr were stained either with a PE-Cy7 Rat IgG2a, kappa isotype control shaded or with the PE-Cy7 Rat Anti-Mouse CD86 antibody unshaded . Right Panel: Freshly isolated unstimulated C57BL/6 splenocytes shaded and LPS-stimulated C57BL/6 splenocytes 72 hr unshaded were stained with the PE-Cy7 Rat Anti-Mouse CD86 antibody. Histograms were derived from gated events based on light scattering characteristics for lymphocytes. Flow cytometry was performed on a BD LSR II flow cytometry system. Show More Flow cytometric analysis of CD86 on mouse splenocytes. Left Panel: LPS-stimulated C57BL/6 splenocytes 72 hr were stained either with a PE-Cy7 Rat IgG2a, kappa isotype control shaded or with the PE-Cy7 Rat Anti-Mouse CD86 antibody unshaded . Right Panel: Freshly isolated unstimulated C57BL/6 splenocytes shaded and LPS-stimulated C57BL/6 splenocytes 72 hr unshaded were stained with the PE-Cy7 Rat Anti-Mouse CD86 antibody. Histograms were derived from gated events based on light scattering characteristics for lymphocytes. Flow cytometry was performed on a BD LSR II flow cytometry system. Flow cytometric analysis of CD86 on mouse splenocytes. Left Panel: LPS-stimulated C57BL/6 splenocytes 72 hr were stained either with a PE-Cy7 Rat IgG2a, kappa isotype control shaded or with the PE-Cy7 Rat Anti-Mouse CD86 antibody unshaded . Right Panel: Freshly isolated unstimulated C57BL/6 splenocytes shaded and LPS-stimulated C57BL/6 splenocytes 72 hr unshaded were stained with the PE-Cy7 Rat Anti-Mouse CD86 antibody. Histograms were derived from gated events based on light scattering characteristics for lymphocytes. Flow cytometry was performed on a BD LSR II flow cytometry system.