ELOVL4 anticorps (C-Term)

N° du produit ABIN5536049

Cet anticorps Lapin Polyclonal détecte spécifiquement ELOVL4 dans WB. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour ELOVL4 anticorps (C-Term) (ABIN5536049)

Antigène: ELOVL4 (ELOVL Fatty Acid Elongase 4 (ELOVL4))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ELOVL4 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ELOVL4 anticorps

Épitope: AA 286-314, C-Term

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

Immunogène: This ELOVL4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 286-314 amino acids from the C-terminal region of human ELOVL4.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: 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: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur ELOVL4

Antigène: ELOVL4 (ELOVL Fatty Acid Elongase 4 (ELOVL4))

Autre désignation: ELOVL4

Sujet: ELOVL4 is a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration.

Poids moléculaire: 37 kDa

ID gène: 6785

UniProt: Q9GZR5