CD59 Polyclonal Antibody
- 货号:GA102580L

Price:
Size:
100 μL
25 μL
Verified Samples |
Verified Samples in WB: Human HUVEC, Human U87-MG, Human Hela Verified Samples in IHC: Human ovary |
Dilution | WB 1:500-1:1000, IHC 1:250-1:500 |
Clonality | Polyclonal |
Isotype | IgG |
Immunogen | Recombinant Human CD59 protein expressed by E.coli |
Abbre | CD59 |
Synonyms | 16.3A5, 1F5, 1F5 antigen, 20 kDa homologous restriction factor, CD 59, CD59, CD59 antigen, CD59 antigen complement regulatory protein , CD59 antigen p18 20, CD59 antigen p18-20 (antigen identified by monoclonal antibodies 16.3A5, CD_antigen=CD59, EJ16, EJ30, EL32 and |
Swissprot | |
Calculated MW | 14 kDa |
Observed MW | 14-17 kDa |
Concentration | 1 mg/mL |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Buffer | PBS with 0.05% proclin 300, 1% protective protein and 50% glycerol,pH7.4 |
Purification Method | Antigen Affinity Purification |
Research Areas | Cancer, Cardiovascular, Immunology, Signal Transduction, Stem Cells |
Conjugation | Unconjugated |
Background | 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. |
Western blot with CD59 Polyclonal antibody at dilution of 1:1000.lane 1:HUVEC whole cell lysate, lane 2:U87-MG whole cell lysate, lane 3:Hela whole cell lysate
Immunohistochemistry of paraffin-embedded Human ovary using CD59 Polyclonal Antibody at dilution of 1:500
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武汉市高新大道858号光谷生物医药产业园二期B18栋