WNT7A anticorps

N° du produit ABIN7261381

Détail du produit anti-WNT7A anticorps

Antigène: WNT7A (Wingless-Type MMTV Integration Site Family, Member 7A (WNT7A))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp WNT7A est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human WNT7A (NP_004616.2).

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000 IF 1:10-1:100

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur WNT7A

Antigène: WNT7A (Wingless-Type MMTV Integration Site Family, Member 7A (WNT7A))

Autre désignation: WNT7A (WNT7A Produits)

Synonymes: anticorps wnt7a, anticorps AI849442, anticorps Wnt-7a, anticorps px, anticorps tw, anticorps Xwnt-7a, anticorps wnt-7a, anticorps wnt7a-A, anticorps Wnt family member 7A, anticorps wingless-type MMTV integration site family, member 7Aa, anticorps wingless-type MMTV integration site family, member 7A, anticorps wingless-type MMTV integration site family member 7A S homeolog, anticorps WNT7A, anticorps wnt7aa, anticorps Wnt7a, anticorps wnt7a.S

Sujet: This gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is involved in the development of the anterior-posterior axis in the female reproductive tract, and also plays a critical role in uterine smooth muscle pattering and maintenance of adult uterine function. Mutations in this gene are associated with Fuhrmann and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromes.

Poids moléculaire:

Observed_MW: 39 kDa

Calculated_MW: 39 kDa

ID gène: 7476

UniProt: O00755

Pathways: Signalisation WNT, Stem Cell Maintenance, Asymmetric Protein Localization