Rabbit Polyclonal antibody to CD59 (CD59 molecule, complement regulatory protein)This gene encodes a cell surface glycoprotein that regulates complement-mediated cell lysis, ａnd it is involved in lymphocyte signal transduction. This protein is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. This protein also plays a role in signal transduction pathways in the activation of T cells. Mutations in this gene cause CD59 deficiency, a disease resulting in hemolytic anemia ａnd thrombosis, ａnd which causes cerebral infarction. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq]
More 

Recombinant protein encompassing a sequence within the center region of human CD59. The exact sequence is proprietary.

IHC-PWB

Human