ALAS2 anticorps (AA 1-190)

N° du produit ABIN7868330

Cet anticorps Lapin Polyclonal détecte spécifiquement ALAS2 dans WB, ELISA, IF et FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour ALAS2 anticorps (AA 1-190) (ABIN7868330)

Antigène: ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALAS2 est non-conjugé

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

Détail du produit anti-ALAS2 anticorps

Épitope: AA 1-190

Fonction: ALAS2 Antibody / ASB / 5-aminolevulinic acid synthase 2

Purification: Antigen affinity purified

Immunogène: Recombinant human protein (amino acids M1-D190) was used as the immunogen for the ALAS2 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the ALAS2 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the ALAS2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur ALAS2

Antigène: ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))

Autre désignation: ALAS2

Sujet: Delta-aminolevulinate synthase 2 also known as ALAS2 is a protein that in humans is encoded by the ALAS2 gene. The product of this gene specifies an erythroid-specific mitochondrially located enzyme. The encoded protein catalyzes the first step in the heme biosynthetic pathway. Defects in this gene cause X-linked pyridoxine-responsive sideroblastic anemia. Alternatively spliced transcript variants encoding different isoforms have been identified.

UniProt: P22557

Pathways: Transition Metal Ion Homeostasis