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AB-108-C, open histogram), followed by Phycoerythrin-conjugated Anti-Goat IgG Secondary Antibody (Catalog # F0107)." class="big_lightbox" target="_blank">
VC004). Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent-Basic (Catalog # CTS013). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to cytoplasm and plasma membrane. View our protocol for IHC Staining with VisUCyte HRP Polymer Detection Reagents." class="big_lightbox" target="_blank">
2519-CD) was serially diluted and captured by Goat Anti-Mouse CD36/SR‑B3 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2519) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Mouse CD36/SR‑B3 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2519) 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" target="_blank">
2519-CD) was serially diluted and captured by Goat Anti-Mouse CD36/SR‑B3 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2519) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Mouse CD36/SR‑B3 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2519) 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" target="_blank">
HAF019). A specific band was detected for CD36/SR-B3 at approximately 85-90 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1." class="big_lightbox" target="_blank">
HAF109). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system." class="big_lightbox" target="_blank">
HAF109). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system." class="big_lightbox" target="_blank">
MAB005, open histogram), followed by Allophycocyanin-conjugated Anti-Rat IgG Secondary Antibody (Catalog # F0113)." class="big_lightbox" target="_blank">
CTS017) and counterstained with hematoxylin (blue). Specific staining was localized to cell surfaces and cytoplasm. View our protocol for Chromogenic IHC Staining of Frozen Tissue Sections." class="big_lightbox" target="_blank">
CTS017) and counterstained with hematoxylin (blue). Specific staining was localized to cell surfaces and cytoplasm. View our protocol for Chromogenic IHC Staining of Frozen Tissue Sections." class="big_lightbox" target="_blank">
CD36 is a cell surface class B scavenger receptor. CD36 is preferentially found within lipid rafts, which facilitates its association with receptors, signalling and adapter molecules. CD36 binds to collagen, thrombospondin, anionic phospholipids and oxidized LDL. CD36 may also function as a cell adhesion molecule and directly mediates cyto adherence of Plasmodium falciparum parasitized erythrocytes. Finally, CD36 binds long chain fatty acids and may function in the transport and/or as a regulator of fatty acid transport.
CD36 has been found to be involved in fatty acid and glucose metabolism, heart disease, taste, and dietary fat processing in the intestine. It may also play roles in glucose intolerance, atherosclerosis, arterial hypertension, diabetes, cardiomyopathy and Alzheimer's disease. CD 36 antibodies are useful tools for studing clucose and fat metabolism or any of the aforementioned diseases.