ETFA anticorps (C-Term)

N° du produit ABIN655079

L’anticorps Lapin Polyclonal anti-ETFA a été validé pour WB, FACS et IHC (p). Il convient pour détecter ETFA dans des échantillons de Humain et Souris.

Aperçu rapide pour ETFA anticorps (C-Term) (ABIN655079)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ETFA est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: RB20724

Détail du produit anti-ETFA anticorps

Épitope: AA 276-304, C-Term

Homologie: B, Pr, Rat

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

Immunogène: This ETFA antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 276-304 amino acids from the C-terminal region of human ETFA.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. IHC-P: 1:50~100. 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 ETFA

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

Autre désignation: ETFA

Sujet: 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.

Poids moléculaire: 35080

ID gène: 2108

NCBI Accession: NP_000117, NP_001121188

UniProt: P13804

Pathways: SARS-CoV-2 Protein Interactome