Anti-CD11b / MAC-1 (Microglial Marker) Monoclonal Antibody(Clone: ITGAM/3338), Clone: [ITGAM/3338], Mouse

Catalog Number: ABI-36-2608-20
Article Name: Anti-CD11b / MAC-1 (Microglial Marker) Monoclonal Antibody(Clone: ITGAM/3338), Clone: [ITGAM/3338], Mouse
Biozol Catalog Number: ABI-36-2608-20
Supplier Catalog Number: 36-2608-20
Alternative Catalog Number: ABI-36-2608-20-20UG
Manufacturer: Abeomics
Host: Mouse
Category: Antikörper
Application: IHC, WB
Species Reactivity: Human
Immunogen: Recombinant fragment (around aa941-1074) of human ITGAM protein (exact sequence is proprietary)
Alternative Names: CD18, CD49d, Cell surface glycoprotein MAC-1 subunit alpha, Complement Component Receptor 3 Alpha, CR3 Alpha Chain (CR3A), Integrin alpha-M, Integrin beta 2 alpha subunit, Leukocyte adhesion receptor MO1, Ly-40, MAC1A, Macrophage antigen alpha polypeptide, MO1A, Neutrophil adherence receptor alpha M
CD11b is a cell adhesion molecule that acts as a receptor for cell surface ligands such as intracellular adhesion molecules (ICAMs) or soluble ligands. Integrins are heterodimeric proteins that contain an a chain and b chain. Integrin aM combines with the Integrin 2 to form a leukocyte-specific integrin referred to as macrophage receptor 1 (Mac-1), or inactivated-C3b (iC3b) receptor 3 (CR3). Integrin aM/2 is important in the adherence of neutrophils and monocytes to stimulated endothelium, and also in the phagocytosis of complement coated particles. The protein CD11b has been implicated in the various adhesion-related interactions of cells such as monocytes, macrophages, natural killer (NK) cells, and granulocytes. It is part of a heterodimer that consists of CD11b andCD18. It also modulates the uptake of complement-coated particles within the cell. It is commonly used as a microglial marker in tissues derived from the nervous system.
Clonality: Monoclonal
Clone Designation: [ITGAM/3338]
NCBI: 3684
UniProt: P11215
Application Dilute: Western Blotting (1-2ug/ml),Immunohistochemistry (Formalin-fixed) (1-2ug/ml for 30 minutes at RT),(Staining of formalin-fixed tissues requires boiling tissue sections in 10mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes),