WIPF1 anticorps

N° du produit ABIN7882693

L’anticorps anti-WIPF1 Polyclonal Lapin est utilisé pour la détection de WIPF1 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB et FACS.

Aperçu rapide pour WIPF1 anticorps (ABIN7882693)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WIPF1 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS)

Détail du produit anti-WIPF1 anticorps

Fonction: WIPF1 Antibody / WASP-interacting protein

Séquence: DSPCEDEWES RFYFHPISDL

Purification: Antigen affinity purified

Immunogène: Amino acids DSPCEDEWESRFYFHPISDL from the human protein were used as the immunogen for the WIPF1 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the WIPF1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the WIPF1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur WIPF1

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

Autre désignation: WIPF1

Sujet: WAS/WASL-interacting protein family member 1, also called 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.

UniProt: O43516

Pathways: Signalisation RTK