EPH Receptor A2 anticorps

N° du produit ABIN7113847

Cet anticorps Souris Monoclonal détecte spécifiquement EPH Receptor A2 dans WB, ELISA et FACS. Il présente une réactivité envers Humain.

Aperçu rapide pour EPH Receptor A2 anticorps (ABIN7113847)

Antigène: EPH Receptor A2 (EPHA2)

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp EPH Receptor A2 est non-conjugé

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

Clone: 2B8

Détail du produit anti-EPH Receptor A2 anticorps

Fonction: EPHA2 antibody

Purification: Protein A+G purification

Pureté: ≥95 % as determined by SDS-PAGE

Immunogène: Ephrin type-A receptor 2

Isotype: IgG1

Information d'application

Indications d'application: WB: 1:2000-1:20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide and 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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur EPH Receptor A2

Antigène: EPH Receptor A2 (EPHA2)

Autre désignation: EPHA2

Sujet:

Synonyms: Ephrin type-A receptor 2|Epithelial cell kinase|Tyrosine-protein kinase receptor ECK|EPHA2|ECK

Background: This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. This gene encodes a protein that binds ephrin-A ligands. Mutations in this gene are the cause of certain genetically-related cataract disorders.

Poids moléculaire: 130 kDa

UniProt: P29317

Pathways: Signalisation RTK