CD59 anticorps (AA 26-102) (FITC)

N° du produit ABIN7977169

L’anticorps anti-CD59 Polyclonal Lapin est utilisé pour la détection de CD59 dans des échantillons de Humain. Il a été validé pour FACS.

Aperçu rapide pour CD59 anticorps (AA 26-102) (FITC) (ABIN7977169)

Antigène: CD59

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CD59 est conjugé à/à la FITC

Application: Flow Cytometry (FACS)

Détail du produit anti-CD59 anticorps (FITC)

Épitope: AA 26-102

Fonction: Anti-CD59 glycoprotein CD59 Antibody FITC Conjugated

Specificité: No cross reactivity with other proteins.

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human CD59 shares 47.1% amino acid (aa) sequence identity with rat CD59.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human CD59 recombinant protein (Position: L26-N102). Human CD59 shares 47.1% amino acid (aa) sequence identity with rat CD59.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur CD59

Antigène: CD59

Autre désignation: CD59

Sujet:

Background: This gene encodes a cell surface glycoprotein that regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction. And 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. It 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.

Gene Full Name: CD59 Molecule (CD59 blood group)

Sequence Similarities: Contains 1 UPAR/Ly6 domain.

ID gène: 966

UniProt: P13987

Pathways: Système du Complément