Anti-CD163 (Monocyte & Macrophage Marker) Monoclonal Antibody(Clone: M130/2162), Clone: [M130/2162], Mouse

Artikelnummer: ABI-36-3552-20
Artikelname: Anti-CD163 (Monocyte & Macrophage Marker) Monoclonal Antibody(Clone: M130/2162), Clone: [M130/2162], Mouse
Artikelnummer: ABI-36-3552-20
Hersteller Artikelnummer: 36-3552-20
Alternativnummer: ABI-36-3552-20-20UG
Hersteller: Abeomics
Wirt: Mouse
Kategorie: Antikörper
Applikation: ELISA, IHC
Spezies Reaktivität: Human
Immunogen: Recombinant fragment (around aa 43-196) of human CD163 (exact sequence is proprietary)
Alternative Synonym: CD163, CD163 antigen, Macrophage-associated antigen, M130, CD163 molecule, Hemoglobin scavenger receptor, MM130, Scavenger receptor cysteine rich type 1 protein M130
This MAb recognizes a protein of 140kDa, identified as CD163. It has been identified as an acute phase-regulated transmembrane protein whose function is to mediate the endocytosis of haptoglobin-hemoglobin complexes. This receptor is expressed on the surface of monocytes with low expression and on tissue macrophages, histiocytes with high expression. Staining with anti-CD163 has been helpful to distinguish synovial macrophages from synovial intimal fibroblasts in rheumatoid arthritis, where its specificity for macrophages was found to be superior to that of anti-CD68. Increased levels of CD163 were also detected in patients with microbial infections and myelomonocytic leukemias. Anti-CD163 is of considerable value for selective identification of monocytes and macrophages at a certain stage of differentiation and is suitable for diagnosing myelomonocytic or monocytic leukaemia and neoplasms of true histiocytic origin. CD163 is positive in skin (histiocytes), gut, Kupffer cells, a few alveolar macrophages, macrophages in the placenta, and in macrophages in inflamed tissues including tumor tissue.
Klonalität: Monoclonal
Klon-Bezeichnung: [M130/2162]
Application Verdünnung: ELISA (For coating, order antibody without BSA),Immunohistochemistry (Formalin-fixed) (1-2ug/ml for 30 minutes at RT)(Staining of formalin-fixed tissues is enhanced by heating tissue sections in 10mM Tris with 1mM EDTA, pH 9.0 for 45 min at 95&degC fo