CD59 antibody (N-Term)

Catalog No. ABIN6991822

This Rabbit Polyclonal antibody specifically detects CD59 in WB and ELISA. It exhibits reactivity toward Human and Mouse.

Quick Overview for CD59 antibody (N-Term) (ABIN6991822)

Target: CD59

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CD59 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-CD59 Antibody

Binding Specificity: N-Term

Purification: CD59 Antibody is affinity chromatography purified via peptide column.

Immunogen: Rabbit polyclonal CD59 antibody was raised against a 14 amino acid peptide near the amino terminus of human CD59. The immunogen is located within the first 50 amino acids of CD59.

Isotype: IgG

Application Details

Application Notes: CD59 antibody can be used for detection of CD59 by Western blot at 1 - 2 μ,g/mL.

Antibody validated: Western Blot in mouse samples. All other applications and species not yet tested.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: CD59 Antibody is supplied in PBS containing 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C,4 °C

Storage Comment: CD59 antibody can be stored at 4°C for three months and -20°C, stable for up to one year.

Target Details for CD59

Target: CD59

Alternative Name: CD59

Background: CD59 Antibody: The complement regulatory protein CD59 is a cell surface glycoprotein that regulates complement-mediated cell lysis and is involved in lymphocyte signal transduction. CD59 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. CD59 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 ultimately cerebral infarction.

Molecular Weight: 14 kDa

Gene ID: 966

NCBI Accession: NP_000602

UniProt: P13987

Pathways: Complement System