WIPF1 anticorps (C-Term) (HRP)

N° du produit ABIN8053924

Cet anticorps anti-WIPF1 Polyclonal Lapin conjugué à HRP (ABIN8053924) détecte spécifiquement WIPF1 dans WB, ELISA et IHC. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour WIPF1 anticorps (C-Term) (HRP) (ABIN8053924)

Antigène: WIPF1 (WAS/WASL Interacting Protein Family, Member 1 (WIPF1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WIPF1 est conjugé à/à la HRP

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

Détail du produit anti-WIPF1 anticorps (HRP)

Épitope: C-Term

Fonction: Anti-WIPF1 Antibody HRP Conjugated

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

Purification: Immunogen affinity purified.

Immunogène: A synthetic peptide corresponding to a sequence at the C-terminus of human WIPF1, which shares 95% amino acid (aa) sequence identity with mouse and rat WIPF1.

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 WIPF1

Antigène: WIPF1 (WAS/WASL Interacting Protein Family, Member 1 (WIPF1))

Autre désignation: WIPF1

Sujet:

Background: WAS/WASL-interacting protein (WIP) is a protein that in humans is encoded by the WIPF1 gene. This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene.

Gene Full Name: WAS/WASL interacting protein family member 1

ID gène: 7456

UniProt: O43516

Pathways: Signalisation RTK