GITR/TNFRSF18 Antibodies

F0102B). View our protocol for Staining Membrane-associated Proteins." class="big_lightbox"> F0102B). View our protocol for Staining Membrane-associated Proteins." alt="RPMI8226 cells (filled histogram) vs. Jurkat cells (open histogram) were stained with Mouse Anti-Human GITR/TNFRSF18 Monoclonal Antibody (Catalog # MAB689) followed by Phycoerythrin-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # F0102B). View our protocol for Staining Membrane-associated Proteins." class="big_thumb" />

689-GR) was serially diluted and captured by Mouse Anti-Human GITR/TNFRSF18 Monoclonal Antibody (Catalog # MAB689) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Human GITR/TNFRSF18 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF689) was biotinylated and incubated with the protein captured on the plate. Detection of the standard curve was achieved by incubating Streptavidin-HRP (Catalog # DY998)" class="big_lightbox"> 689-GR) was serially diluted and captured by Mouse Anti-Human GITR/TNFRSF18 Monoclonal Antibody (Catalog # MAB689) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Human GITR/TNFRSF18 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF689) was biotinylated and incubated with the protein captured on the plate. Detection of the standard curve was achieved by incubating Streptavidin-HRP (Catalog # DY998)" class="big_thumb" />

CTS008) and counterstained with hematoxylin (blue). Specific staining was localized to trabeculae sinuses . View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections." class="big_lightbox"> CTS008) and counterstained with hematoxylin (blue). Specific staining was localized to trabeculae sinuses . View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections." alt="GITR/TNFRSF18 was detected in immersion fixed paraffin-embedded sections of human tonsil using Goat Anti-Human GITR/TNFRSF18 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF689) at 10 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS008) and counterstained with hematoxylin (blue). Specific staining was localized to trabeculae sinuses . View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections." class="big_thumb" />

689-GR) was serially diluted and captured by Mouse Anti-Human GITR/TNFRSF18 Monoclonal Antibody (Catalog # MAB689) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Human GITR/TNFRSF18 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF689) was biotinylated and incubated with the protein captured on the plate. Detection of the standard curve was achieved by incubating Streptavidin-HRP (Catalog # DY998)" class="big_lightbox"> 689-GR) was serially diluted and captured by Mouse Anti-Human GITR/TNFRSF18 Monoclonal Antibody (Catalog # MAB689) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Human GITR/TNFRSF18 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF689) was biotinylated and incubated with the protein captured on the plate. Detection of the standard curve was achieved by incubating Streptavidin-HRP (Catalog # DY998)" class="big_thumb" />

F0111). Quadrant markers were set based on control antibody staining (Catalog # MAB1050). View our protocol for Staining Membrane-associated Proteins." class="big_lightbox"> F0111). Quadrant markers were set based on control antibody staining (Catalog # MAB1050). View our protocol for Staining Membrane-associated Proteins." alt="HEK293 human embryonic kidney cell line transfected with (A) mouse GITR/TNFRSF18 or (B) irrelevant transfectants and eGFP was stained with Rabbit Anti-Mouse GITR/TNFRSF18 Monoclonal Antibody (Catalog # MAB52412) followed by APC-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog # F0111). Quadrant markers were set based on control antibody staining (Catalog # MAB1050). View our protocol for Staining Membrane-associated Proteins." class="big_thumb" />

NL004) and counterstained with DAPI (blue). Specific staining was localized to cell surfaces. View our protocol for Fluorescent ICC Staining of Non-adherent Cells." class="big_lightbox"> NL004) and counterstained with DAPI (blue). Specific staining was localized to cell surfaces. View our protocol for Fluorescent ICC Staining of Non-adherent Cells." class="big_thumb" />

VC003). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to lymphocytes. View our protocol for IHC Staining with VisUCyte HRP Polymer Detection Reagents." class="big_lightbox"> VC003). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to lymphocytes. View our protocol for IHC Staining with VisUCyte HRP Polymer Detection Reagents." class="big_thumb" />