Sample Preparation
Cell Separation
Flow Cytometry
Cell Culture&Stimulation
Cell manufacturing
Imaging and Microscopy
MACSmolecular
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CD56 + and CD14 + cells were isolated with CD56 MicroBeads and CD14 MicroBeads from human peripheral blood cells (PBMCs). CD56 + NK cells were stimulated with CD14 + monocytes and 1 ng/mL human IL-2 for 3 days. Cells were stained with CD336 (NKp44) antibodies or with the corresponding REA Control (S) antibodies (left images) as well as with CD56 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. The Tandem Signal Enhancer has been used to increase binding specificity of tandem-dye–conjugated antibodies. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence or 4',6-diamidino-2-phenylindole (DAPI) fluorescence, as in the case of tandem conjugates. |