BD Pharmingen- HiCK-3 Human Cytokine Positive Control Cells_BD Pharmingen
参考图片
Flow cytometric staining of HiCK-3 Human Cytokine Positive Cells for IL-1α, IL-1β, IL-6, IL-12 and TNF. HiCK-3 cells were washed, permeabilized, and subsequently stained with either a PE-conjugated isotype control (upper far left panel), PE Mouse Anti-Human IL-1α (upper left middle panel, Cat. No. 554561), PE Mouse Anti-Human IL-1β (upper right middle panel, Cat. No. 340516), PE Rat Anti-Human IL-6 (upper far right panel, Cat. No. 554697), PE Mouse Anti-Human IL-12p40/p70 (lower far left panel, Cat. No. 554575), PE Rat Anti-Human IL-12 p70 (lower left middle panel, Cat. No. 557020), or PE Mouse Anti-Human TNF (lower right middle panel, Cat. No. 554513). Despite fixation and freezing, the side- and forward scattered light signals for these control cells (see far lower right panel) remain similar to those for freshly-prepared lymphoid cell preparations (data not shown). Quadrant markers were set based on the autofluorescence controls to calculate the percentages of cells contained in each quadrant region as shown.
Flow cytometric staining of HiCK-3 Human Cytokine Positive Cells for IL-1α, IL-1β, IL-6, IL-12 and TNF. HiCK-3 cells were washed, permeabilized, and subsequently stained with either a PE-conjugated isotype control (upper far left panel), PE Mouse Anti-Human IL-1α (upper left middle panel, Cat. No. 554561), PE Mouse Anti-Human IL-1β (upper right middle panel, Cat. No. 340516), PE Rat Anti-Human IL-6 (upper far right panel, Cat. No. 554697), PE Mouse Anti-Human IL-12p40/p70 (lower far left panel, Cat. No. 554575), PE Rat Anti-Human IL-12 p70 (lower left middle panel, Cat. No. 557020), or PE Mouse Anti-Human TNF (lower right middle panel, Cat. No. 554513). Despite fixation and freezing, the side- and forward scattered light signals for these control cells (see far lower right panel) remain similar to those for freshly-prepared lymphoid cell preparations (data not shown). Quadrant markers were set based on the autofluorescence controls to calculate the percentages of cells contained in each quadrant region as shown.
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