F0105B) and Rat Anti-Mouse CD4 APC-conjugated Monoclonal Antibody (
FAB554A). Quadrant markers were set based on control antibody staining (
MAB006). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (
FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (
FC005). View our protocol for
Staining Intracellular Molecules." class="big_lightbox">

F0105B) and Rat Anti-Mouse CD4 APC-conjugated Monoclonal Antibody (
FAB554A). Quadrant markers were set based on control antibody staining (
MAB006). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (
FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (
FC005). View our protocol for
Staining Intracellular Molecules." alt="Mouse splenocytes either (A) stimulated to induce Th1 cells or (B) unstimulated were stained with Rat Anti-Mouse IFN-gamma Monoclonal Antibody (Catalog # MAB485) followed by Phycoerythrin-conjugated Anti-Rat IgG Secondary Antibody (
F0105B) and Rat Anti-Mouse CD4 APC-conjugated Monoclonal Antibody (
FAB554A). Quadrant markers were set based on control antibody staining (
MAB006). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (
FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (
FC005). View our protocol for
Staining Intracellular Molecules." class="big_thumb" />
5476) or (B) unstimulated were stained with Rat Anti-Mouse IFN-gamma Monoclonal Antibody (Catalog # MAB485) followed by Phycoerythrin-conjugated Anti-Rat IgG Secondary Antibody (
F0105B) and Rat Anti-Mouse CD4 APC-conjugated Monoclonal Antibody (
FAB554A). Quadrant markers were set based on control antibody staining (
MAB006). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (
FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (
FC005). Staining was performed using our Staining Intracellular Molecules protocol." class="big_lightbox">

5476) or (B) unstimulated were stained with Rat Anti-Mouse IFN-gamma Monoclonal Antibody (Catalog # MAB485) followed by Phycoerythrin-conjugated Anti-Rat IgG Secondary Antibody (
F0105B) and Rat Anti-Mouse CD4 APC-conjugated Monoclonal Antibody (
FAB554A). Quadrant markers were set based on control antibody staining (
MAB006). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (
FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (
FC005). Staining was performed using our Staining Intracellular Molecules protocol." class="big_thumb" />
485-MI) reduces the Encephalomyocarditis Virus (EMCV)-induced cytopathy in the L-929 mouse fibroblast cell line in a dose-dependent manner (orange line), as measured by crystal violet staining. Inhibition of EMCV activity elicited by Recombinant Mouse IFN-gamma (2.5 ng/mL) is neutralized (green line) by increasing concentrations of Rat Anti-Mouse IFN-gamma Monoclonal Antibody (Catalog # MAB485). The ND
50 is typically 0.075-0.3 µg/mL." class="big_lightbox">

485-MI) reduces the Encephalomyocarditis Virus (EMCV)-induced cytopathy in the L-929 mouse fibroblast cell line in a dose-dependent manner (orange line), as measured by crystal violet staining. Inhibition of EMCV activity elicited by Recombinant Mouse IFN-gamma (2.5 ng/mL) is neutralized (green line) by increasing concentrations of Rat Anti-Mouse IFN-gamma Monoclonal Antibody (Catalog # MAB485). The ND
50 is typically 0.075-0.3 µg/mL." class="big_thumb" />
VC005). Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using VisUCyte Antigen Retrieval Reagent-Basic (Catalog #
VCTS021). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to cytoplasm in lymphocytes. View our protocol for
IHC Staining with VisUCyte HRP Polymer Detection Reagents." class="big_lightbox">

VC005). Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using VisUCyte Antigen Retrieval Reagent-Basic (Catalog #
VCTS021). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to cytoplasm in lymphocytes. View our protocol for
IHC Staining with VisUCyte HRP Polymer Detection Reagents." class="big_thumb" />