ETFA anticorps (AA 1-333)

N° du produit ABIN7869204

L’anticorps anti-ETFA Polyclonal Lapin est utilisé pour la détection de ETFA dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, ELISA, IF et IHC (p).

Aperçu rapide pour ETFA anticorps (AA 1-333) (ABIN7869204)

Antigène: ETFA (Electron-Transfer-Flavoprotein, alpha Polypeptide (ETFA))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ETFA est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-ETFA anticorps

Épitope: AA 1-333

Fonction: ETFA Antibody

Purification: Antigen affinity purified

Immunogène: Recombinant human protein (amino acids M1-K333) was used as the immunogen for the ETFA antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the ETFA 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 ETFA 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 ETFA

Antigène: ETFA (Electron-Transfer-Flavoprotein, alpha Polypeptide (ETFA))

Autre désignation: ETFA

Sujet: The human ETFA gene encodes the Electron-transfer-flavoprotein, alpha subunit, also known as ETF-a. Together with Electron-transfer-flavoprotein, beta subunit, encoded by the 'ETFB' gene, it forms the heterodimeric Electron transfer flavoprotein (ETF). ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene.

UniProt: P13804

Pathways: SARS-CoV-2 Protein Interactome