BD PharmingenTM PE Rat anti-Mouse CD107a

Description

Flow cytometric analysis of PE-conjugated anti-mouse CD107a on mouse splenocytes. Murine splenocytes were permeabilized with BD Cytofix/Cytoperm fixation/permeabilization buffer Cat. No.554722 and then stained with either PE anti-CD107a clone 1D4B, Cat. No. 558661, solid line or a PE rat IgG2a isotype control catalog number 553930, dashed line . Intracellular staining was analysed by flow cytometry performed on a BD FACSCalibur System. The histograms were derived from the gated events based on light scattering characteristics of viable splenocytes. Flow cytometric analysis of PE-conjugated anti-mouse CD107a on mouse splenocytes. Murine splenocytes were permeabilized with BD Cytofix/Cytoperm fixation/permeabilization buffer Cat. No.554722 and then stained with either PE anti-CD107a clone 1D4B, Cat. No. 558661, solid line or a PE rat IgG2a isotype control catalog number 553930, dashed line . Intracellular staining was analysed by flow cytometry performed on a BD FACSCalibur System. The histograms were derived from the gated events based on light scattering characteristics of viable splenocytes. Show More Flow cytometric analysis of PE-conjugated anti-mouse CD107a on mouse splenocytes. Murine splenocytes were permeabilized with BD Cytofix/Cytoperm fixation/permeabilization buffer Cat. No.554722 and then stained with either PE anti-CD107a clone 1D4B, Cat. No. 558661, solid line or a PE rat IgG2a isotype control catalog number 553930, dashed line . Intracellular staining was analysed by flow cytometry performed on a BD FACSCalibur System. The histograms were derived from the gated events based on light scattering characteristics of viable splenocytes.