Ectodysplasin A anticorps (Middle Region)

N° du produit ABIN634516

Cet anticorps Lapin Polyclonal détecte spécifiquement Ectodysplasin A dans WB. Il présente une réactivité envers Humain, Souris, Rat et Chien.

Aperçu rapide pour Ectodysplasin A anticorps (Middle Region) (ABIN634516)

Antigène: Ectodysplasin A (EDA)

Reactivité: Humain, Souris, Rat, Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Ectodysplasin A est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Ectodysplasin A anticorps

Épitope: Middle Region

Specificité: Ectodysplasin A antibody was raised against the middle region of EDA

Purification: Affinity purified

Immunogène: Ectodysplasin A antibody was raised using the middle region of EDA corresponding to a region with amino acids GPPGPPGPQGPPGLQGPSGAADKAGTRENQPAVVHLQGQGSAIQVKNDLS

Information d'application

Indications d'application: WB: 1 µg/mL
Optimal conditions should be determined by the investigator.

Commentaires:

Ectodysplasin A Blocking Peptide, (ABIN938863), is also available for use as a blocking control in assays to test for specificity of this Ectodysplasin A antibody

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Lyophilized powder. Add distilled water for a 1 mg/mL concentration of EDA antibody in PBS

Concentration: Lot specific

Buffer: PBS

Conseil sur la manipulation: Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.

Détails sur Ectodysplasin A

Antigène: Ectodysplasin A (EDA)

Autre désignation: Ectodysplasin A

Sujet: EDA is a type II membrane protein that can be cleaved by furin to produce a secreted form. It belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene.

Poids moléculaire: 41 kDa (MW of target protein)

Pathways: Tube Formation