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CD24 + cells were depleted from the CML cell line K562 using the CD24 MicroBead Kit, an LD Column, and a QuadroMACS™ Separator. Cells were fluorescently labeled with CD24-PE and analyzed by flow cytometry using the MACSQuant® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
A: | B: |
Unseparated fraction | CD24 - cell fraction |
CD24 MicroBead Kit, humanFigure 1CD24 + cells were depleted from the CML cell line K562 using the CD24 MicroBead Kit, an LD Column, and a QuadroMACS™ Separator. Cells were fluorescently labeled with CD24-PE and analyzed by flow cytometry using the MACSQuant® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | CD24 MicroBead Kit, humanFigure 1CD24 + cells were depleted from the CML cell line K562 using the CD24 MicroBead Kit, an LD Column, and a QuadroMACS™ Separator. Cells were fluorescently labeled with CD24-PE and analyzed by flow cytometry using the MACSQuant® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
CD24 + cells were depleted from the CML cell line K562 using the CD24 MicroBead Kit, an LD Column, and a QuadroMACS™ Separator. Cells were fluorescently labeled with CD24-PE and analyzed by flow cytometry using the MACSQuant® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
A: | B: |
Unseparated fraction | CD24 - cell fraction |
CD24 MicroBead Kit, humanFigure 1CD24 + cells were depleted from the CML cell line K562 using the CD24 MicroBead Kit, an LD Column, and a QuadroMACS™ Separator. Cells were fluorescently labeled with CD24-PE and analyzed by flow cytometry using the MACSQuant® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | CD24 MicroBead Kit, humanFigure 1CD24 + cells were depleted from the CML cell line K562 using the CD24 MicroBead Kit, an LD Column, and a QuadroMACS™ Separator. Cells were fluorescently labeled with CD24-PE and analyzed by flow cytometry using the MACSQuant® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
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