Endoglin anticorps (AA 265-294)

N° du produit ABIN655186

Cet anticorps Lapin Polyclonal détecte spécifiquement Endoglin dans WB et FACS. Il présente une réactivité envers Humain.

Aperçu rapide pour Endoglin anticorps (AA 265-294) (ABIN655186)

Antigène: Endoglin (ENG)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Endoglin est non-conjugé

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

Clone: RB20948

Détail du produit anti-Endoglin anticorps

Épitope: AA 265-294

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This ENG antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 265-294 amino acids from the Central region of human ENG.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. FC: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur Endoglin

Antigène: Endoglin (ENG)

Autre désignation: ENG

Sujet: This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds TGFB1 and TGFB3 with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Poids moléculaire: 70578

ID gène: 2022

NCBI Accession: NP_000109, NP_001108225, NP_001265067

UniProt: P17813