F0111) and Mouse anti-Human CD14 PE-conjugated Monoclonal Antibody (Catalog #
FAB3832P). Quadrant markers were set based on isotype control antibody staining (Catalog #
MAB1050, data not shown). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog #
FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog #
FC005). View our protocol for
Staining Intracellular Molecules." class="big_lightbox">

F0111) and Mouse anti-Human CD14 PE-conjugated Monoclonal Antibody (Catalog #
FAB3832P). Quadrant markers were set based on isotype control antibody staining (Catalog #
MAB1050, data not shown). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog #
FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog #
FC005). View our protocol for
Staining Intracellular Molecules." alt="Human peripheral blood monocytes, either (A) untreated, or (B) treated with 500 ng/mL LPS overnight, were stained with Rabbit anti-Human IL-1 beta/IL-1F2 Monoclonal Antibody (Catalog # MAB8406) followed by APC-conjugated anti-Rabbit IgG secondary antibody (Catalog #
F0111) and Mouse anti-Human CD14 PE-conjugated Monoclonal Antibody (Catalog #
FAB3832P). Quadrant markers were set based on isotype control antibody staining (Catalog #
MAB1050, data not shown). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog #
FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog #
FC005). View our protocol for
Staining Intracellular Molecules." class="big_thumb" />