nectin-3 anticorps (AA 92-296)

N° du produit ABIN7877170

Cet anticorps anti-nectin-3 Polyclonal Lapin (ABIN7877170) détecte spécifiquement nectin-3 dans WB, ELISA, FACS et IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour nectin-3 anticorps (AA 92-296) (ABIN7877170)

Antigène: nectin-3 (NECTIN3) (Nectin cell adhesion molecule 3 (NECTIN3))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp nectin-3 est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-nectin-3 anticorps

Épitope: AA 92-296

Fonction: Nectin 3 Antibody

Purification: Affinity purified

Immunogène: Recombinant human protein (amino acids E92-N296) was used as the immunogen for the Nectin 3 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Nectin 3 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 Nectin 3 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 nectin-3

Antigène: nectin-3 (NECTIN3) (Nectin cell adhesion molecule 3 (NECTIN3))

Autre désignation: Nectin 3

Sujet: Nectin-3, also known as poliovirus receptor-related 3, is a 95 kDa type I transmembrane glycoprotein belonging to the Nectin family of Ig superfamily proteins. It is mapped to 3q13.13. This gene encodes a member of the nectin family of proteins, which function as adhesion molecules at adherens junctions. This family member interacts with other nectin-like proteins and with afadin, a filamentous actin-binding protein involved in the regulation of directional motility, cell proliferation and survival. This gene plays a role in ocular development involving the ciliary body. Mutations in this gene are believed to result in congenital ocular defects. Alternative splicing results in multiple transcript variants.

UniProt: Q9NQS3

Pathways: Cell-Cell Junction Organization