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BD PharmingenTM PE Mouse anti-Human IFN-alpha[2b]

560097 ·

BDB Bioscience · Cat: 560097

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Catalog No: 560097
Category: reagents
Brand: BDB Bioscience

Description

Flow cytometric analysis of PE anti-human IFN alpha on stimulated PBMC. Human PBMC were stimulated using CPG oligodeoxynucleotide and then treated with BFA. Cells were then stained with FITC conjugated Lin-1 cocktail, PerCP-Cy5.5 Mouse anti-Human CD123, and APC Mouse Anti-Human HLA-DR simutaneously. Cells were fixed and permeabilized see recommended assay procedure followed by intracellular staining with PE anti-human IFN-alpha. The dot plots were derived from the gated events based on light scattering characteristics of lymphocytes and fluorescence characteristics of Lin-1 negative, HLDA-DR positive shown as IFN-alpha vs CD123. Flow cytometry was performed on a BD FACSCalibur System. Please refer to Recommended Assay Procedure for a full protocol and list of materials Flow cytometric analysis of PE anti-human IFN alpha on stimulated PBMC. Human PBMC were stimulated using CPG oligodeoxynucleotide and then treated with BFA. Cells were then stained with FITC conjugated Lin-1 cocktail, PerCP-Cy5.5 Mouse anti-Human CD123, and APC Mouse Anti-Human HLA-DR simutaneously. Cells were fixed and permeabilized see recommended assay procedure followed by intracellular staining with PE anti-human IFN-alpha. The dot plots were derived from the gated events based on light scattering characteristics of lymphocytes and fluorescence characteristics of Lin-1 negative, HLDA-DR positive shown as IFN-alpha vs CD123. Flow cytometry was performed on a BD FACSCalibur System. Please refer to Recommended Assay Procedure for a full protocol and list of materials Show More Flow cytometric analysis of PE anti-human IFN alpha on stimulated PBMC. Human PBMC were stimulated using CPG oligodeoxynucleotide and then treated with BFA. Cells were then stained with FITC conjugated Lin-1 cocktail, PerCP-Cy5.5 Mouse anti-Human CD123, and APC Mouse Anti-Human HLA-DR simutaneously. Cells were fixed and permeabilized see recommended assay procedure followed by intracellular staining with PE anti-human IFN-alpha. The dot plots were derived from the gated events based on light scattering characteristics of lymphocytes and fluorescence characteristics of Lin-1 negative, HLDA-DR positive shown as IFN-alpha vs CD123. Flow cytometry was performed on a BD FACSCalibur System. Please refer to Recommended Assay Procedure for a full protocol and list of materials

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