ELISA CD59 anti-

Quantity :50µL Clone Number: Aliases:16.3A5 antibody; 1F5 antibody; 1F5 antigen antibody; 20 kDa homologous restriction factor antibody; CD 59 antibody; CD_antigen=CD59 antibody; CD59 antibody; CD59 antigen antibody; CD59 antigen complement regµLatory protein antibody; CD59 antigen p18 20 antibody; CD59 antigen p18-20 (antigen identified by monoclonal antibodies 16.3A5; EJ16; EJ30; EL32 and G344) antibody; CD59 glycoprotein antibody; CD59 molecµLe antibody; CD59 molecµLe complement regµLatory protein antibody; CD59_ antibody; Cd59a antibody; Complement regµLatory protein antibody; EJ16 antibody; EJ30 antibody; EL32 antibody; FLJ38134 antibody; FLJ92039 antibody; G344 antibody; HRF 20 antibody; HRF-20 antibody; HRF20 antibody; leukocyte antigen MIC11 antibody; Ly 6 like protein antibody; Lymphocytic antigen CD59/MEM43 antibody; MAC inhibitory protein antibody; MAC IP antibody; MAC-inhibitory protein antibody; MAC-IP antibody; MACIF antibody; MACIP antibody; MEM43 antibody; MEM43 antigen antibody; Membrane attack complex (MAC) inhibition factor antibody; Membrane attack complex inhibition factor antibody; Membrane inhibitor of reactive lysis antibody; MGC2354 antibody; MIC11 antibody; MIN1 antibody; MIN2 antibody; MIN3 antibody; MIRL antibody; MSK21 antibody; p18 20 antibody; Protectin antibody; Surface antigen recognized by monoclonal antibody 16.3A5 antibody; T cell activating protein antibody Product Type:Polyclonal Antibody Immunogen Species:Homo sapiens () UniProt ID:P13987 Immunogen:Synthetic peptide of CD59 Raised in:Rabbit Reactivity: Tested Applications:ELISA, WB, IHC; ELISA:1:2000-1:10000, WB:1:500-1:2000, IHC:1:100-1:300 Background:This gene encodes a cell surface glycoprotein that regµLates 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 mµLtiple 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 resµLting in hemolytic anemia and thrombosis, and which causes cerebral infarction. Clonality:Polyclonal Isotype:IgG Purification Method:Antigen affinity purification Conjµgate:Non-conjµgated Buffer:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol Form:Liquid Stroage:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. Target Names:CD59 Research Areas:CardiovascµLar;Immunology;Signal transduction?Stem cells