NDUFAF2 anticorps (PE-Cy5.5)

N° du produit ABIN906406

Cet anticorps Lapin Polyclonal détecte spécifiquement NDUFAF2 dans WB. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour NDUFAF2 anticorps (PE-Cy5.5) (ABIN906406)

Antigène: NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NDUFAF2 est conjugé à/à la PE-Cy5.5

Application: Western Blotting (WB)

Détail du produit anti-NDUFAF2 anticorps (PE-Cy5.5)

Homologie: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human Mimitin

Isotype: IgG

Information d'application

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur NDUFAF2

Antigène: NDUFAF2 (NADH Dehydrogenase (Ubiquinone) 1 alpha Subcomplex, Assembly Factor 2 (NDUFAF2))

Autre désignation: Mimitin

Sujet:

Synonyms: mitochondrial, B17.2 like, B17.2-like, B17.2L, MIMIT_HUMAN, Mimitin, Mimitin mitochondrial, MMTN, Myc induced mitochondrial protein, Myc-induced mitochondrial protein, NADH dehydrogenase ubiquinone 1 alpha subcomplex assembly factor 2, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2, NDUFA12 like, NDUFA12 like protein, NDUFA12-like protein, NDUFA12L, NDUFAF2.

Background: NADH:ubiquinone oxidoreductase (complex I) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene cause progressive encephalopathy resulting from mitochondrial complex I deficiency.

Poids moléculaire: 20kDa

Pathways: SARS-CoV-2 Protein Interactome