The Anti-CD36 Chimeric Recombinant Rabbit Monoclonal Antibody (HDAB0231) is a cutting-edge tool for researchers studying the CD36 protein, which plays a critical role in lipid metabolism, atherosclerosis, and inflammation. This monoclonal antibody, developed using advanced chimeric technology, offers high specificity and sensitivity in detecting and analyzing CD36 in various cell types and tissues.CD36, a multifunctional scavenger receptor, is known for its involvement in fatty acid uptake, cellular signaling, and inflammation regulation. Dysregulation of CD36 has been implicated in metabolic disorders, cardiovascular diseases, and inflammatory conditions.
This antibody provides a reliable means of studying CD36 expression and function, making it an invaluable asset in lipid metabolism research, atherosclerosis studies, and inflammatory disease investigations.With its exceptional specificity and performance in various applications such as immunofluorescence, immunohistochemistry, and flow cytometry, the Anti-CD36 Chimeric Recombinant Rabbit Monoclonal Antibody (HDAB0231) promises to enhance the accuracy and efficiency of research efforts focusing on the intricate roles of CD36 in health and disease.
Purified from cell culture supernatant by affinity chromatography
Formulation:
Powder
Buffer:
1XPBS
Storage:
Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing).Lyophilized antibodies are shipped at ambient temperature.
Usage:
Research use only
Background:
The protein encoded by this gene is the fourth major glycoprotein of the platelet surface and serves as a receptor for thrombospondin in platelets and various cell lines. Since thrombospondins are widely distributed proteins involved in a variety of adhesive processes, this protein may have important functions as a cell adhesion molecule. It binds to collagen, thrombospondin, anionic phospholipids and oxidized LDL. It directly mediates cytoadherence of Plasmodium falciparum parasitized erythrocytes and it binds long chain fatty acids and may function in the transport and/or as a regulator of fatty acid transport. Mutations in this gene cause platelet glycoprotein deficiency. Multiple alternatively spliced transcript variants have been found for this gene.
