ITGA7 anticorps (AA 229-257)

N° du produit ABIN3031400

L’anticorps Lapin Polyclonal anti-ITGA7 a été validé pour WB et ELISA. Il convient pour détecter ITGA7 dans des échantillons de Humain.

Aperçu rapide pour ITGA7 anticorps (AA 229-257) (ABIN3031400)

Antigène: ITGA7 (Integrin, alpha 7 (ITGA7))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ITGA7 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-ITGA7 anticorps

Épitope: AA 229-257

Réactivité croisée (Details): Expected species reactivity: Mouse

Purification: Antigen affinity purified

Immunogène: A portion of amino acids 229-257 from the human protein was used as the immunogen for this Integrin alpha 7 antibody.

Isotype: Ig Fraction

Information d'application

Indications d'application: Titration of the Integrin alpha 7 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

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: Aliquot the Integrin alpha 7 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Détails sur ITGA7

Antigène: ITGA7 (Integrin, alpha 7 (ITGA7))

Autre désignation: Integrin alpha 7

Sujet: The protein encoded by this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. They mediate a wide spectrum of cell-cell and cell-matrix interactions, and thus play a role in cell migration, morphologic development, differentiation, and metastasis. This protein functions as a receptor for the basement membrane protein laminin-1. It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis. Defects in this gene are associated with congenital myopathy. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

UniProt: Q13683

Pathways: Integrin Complex