ETFA anticorps (C-Term)

N° du produit ABIN952127

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

Aperçu rapide pour ETFA anticorps (C-Term) (ABIN952127)

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)), Enzyme Immunoassay (EIA)

Détail du produit anti-ETFA anticorps

Épitope: AA 283-311, C-Term

Specificité: This antibody recognizes Human and Mouse ETFA (C-term).

Purification: Affinity Chromatography on Protein A

Immunogène: KLH conjugated synthetic peptide between 283-311 amino acids from the C-terminal region of human ETFA

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

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.Synonyms: Alpha-ETF, Electron transfer flavoprotein subunit alpha

Poids moléculaire: 35080 Da

ID gène: 2108

NCBI Accession: NP_000117

Pathways: SARS-CoV-2 Protein Interactome