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Name :
Recombinant Human CD59 Protein, MYC/DDK-tagged

Specification :
| Description : 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. | Source : HEK293 | Species : Human | Tag : MYC/DDK | Form : 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol. | Molecular Mass : 11.6 kDa | Purity : > 80% as determined by SDS-PAGE and Coomassie blue staining | Concentration : >50 ug/mL as determined by microplate BCA method

Gene Information :
| Gene Name : CD59 CD59 molecule, complement regulatory protein [ Homo sapiens ] | Official Symbol : CD59 | Synonyms : 16.3A5; 1F5; EJ16; EJ30; EL32; G344; HRF-20; HRF20; MAC-IP; MACIF; MEM43; MIC11; MIN1; MIN2; | Gene ID : 966 | mRNA Refseq : NM_000611 | Protein Refseq : NP_000602 | MIM : 107271 | UniProt ID : P13987

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Author: Cholesterol Absorption Inhibitors