Allophycocyanin apc cy7 conjugated anti human cd3

Recombinant human IL-2 and IL-15 (PeproTech, Rocky Hill, NJ, USA) were used to expand NK cells from PBMCs. Allophycocyanin (APC)-Cy7-conjugated anti-human CD3, phycoerythrin (PE)-Cy7-conjugated anti-human CD56, PE-Cy5-conjugated CD56, and fluorescein isothiocyanate (FITC)-conjugated CD3 (eBioscience, San Diego, CA, USA) were used to measure NK cell purity (CD56+/CD3–). Pacific blue-conjugated anti-human CD16, FITC-conjugated anti-human CD57, APC-conjugated anti-human DNAM-1, peridinin chlorophyll protein complex (PerCP)-conjugated anti-human NKG2D, PE-conjugated anti-human NKG2C, APC-conjugated anti-human NKG2A, and PE-conjugated anti-human NKp30, PerCP-Cyanine5.5-conjugated anti-human NKp44, Pacific blue-conjugated anti-human NKp46 (eBioscience), PerCP-Cyanine5.5-conjugated anti-human KIR2DL1, FITC-conjugated anti-human KIR2DL2/3, and Pacific blue-conjugated anti-human KIR3DL1 (BD Biosciences, Franklin Lakes, NJ, USA) were used to measure expanded NK cell receptor levels. BV421-conjugated anti-human IFN-γ and APC-conjugated anti-human TNF-α (BD Biosciences) were used for intracellular staining, and PE-conjugated anti-human CD107a (BD Biosciences) was used as a surrogate marker for degranulation.

Recombinant human interleukin (IL)-2 and IL-15 (PeproTech, Rocky Hill, NJ, USA) were used to expand NK cells. Phycoerythrin (PE)-conjugated anti-human HLA-E (clone 3D12) (BioLegend, San Diego, CA, USA) was used to measure HLA-E expression on generically modified K562-HLA-E during culture. Allophycocyanin (APC)-Cy7-conjugated anti-human CD3, PE-Cy7-conjugated anti-human CD56, pacific blue-conjugated anti-human CD16, fluorescein isothiocyanate (FITC)-conjugated anti-human CD57, pacific blue-conjugated anti-human NKp46, PE-conjugated anti-human NKp30, peridinin chlorophyll protein complex (PerCP)-conjugated anti-human NKG2D (eBioscience, San Diego, CA, USA), FITC-conjugated anti-human CD69, APC-conjugated anti-human DNAM-1 (BD Biosciences, San Jose, CA, USA), APC-conjugated anti-human NKG2A, PE-conjugated anti-human NKG2C, PerCP-conjugated anti-human KIR2DL1 (R & D Systems, Minneapolis, MN, USA), FITC-conjugated anti-human KIR2DL2/L3, and BV421-conjugated anti-human KIR3DL1 (BioLegend) were used to evaluate purity and surface expression of NK cell receptors. The PE-conjugated anti-human CD107a mAb was used as a surrogate marker for quantifying degranulation. BV421-conjugated anti-human interferon (IFN)-γ and FITC-conjugated anti-FcεRIγ subunit (FcɛRγ) (Millipore, CA, USA) were used for intracellular staining.