FZD9 anticorps (AA 27-591) (HRP)

N° du produit ABIN7991885

Cet anticorps anti-FZD9 Polyclonal Lapin conjugué à HRP (ABIN7991885) détecte spécifiquement FZD9 dans WB, ELISA et IHC. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour FZD9 anticorps (AA 27-591) (HRP) (ABIN7991885)

Antigène: FZD9 (Frizzled Family Receptor 9 (FZD9))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FZD9 est conjugé à/à la HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Détail du produit anti-FZD9 anticorps (HRP)

Épitope: AA 27-591

Fonction: Anti-Frizzled 9/FZD9 Antibody HRP Conjugated

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

Homologie: Human Frizzled 9,FZD9 shares 95.9%,96.1% amino acid (aa) sequence identity with mouse,rat Frizzled 9,FZD9,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human Frizzled 9/FZD9 recombinant protein (Position: R27-L591). Human Frizzled 9/FZD9 shares 95.9% and 96.1% amino acid (aa) sequence identity with mouse and rat Frizzled 9/FZD9, respectively.

Isotype: IgG

Information d'application

Indications d'application: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, 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.

Stock: -20 °C

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

Date de péremption: 12 months

Détails sur FZD9

Antigène: FZD9 (Frizzled Family Receptor 9 (FZD9))

Autre désignation: FZD9

Sujet:

Background: Members of the 'frizzled' gene family encode 7-transmembrane domain proteins that are receptors for Wnt signaling proteins. The FZD9 gene is located within the Williams syndrome common deletion region of chromosome 7, and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype. FZD9 is expressed predominantly in brain, testis, eye, skeletal muscle, and kidney.

Gene Full Name: frizzled class receptor 9

ID gène: 8326

UniProt: O00144

Pathways: Signalisation WNT