COX17 anticorps

N° du produit ABIN7248020

Cet anticorps Lapin Polyclonal détecte spécifiquement COX17 dans ELISA et IHC. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour COX17 anticorps (ABIN7248020)

Antigène: COX17 (COX17 Cytochrome C Oxidase Assembly Protein 17 (COX17))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp COX17 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Détail du produit anti-COX17 anticorps

Attributs du produit: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogène: Synthetic peptide of human COX17

Isotype: IgG

Information d'application

Indications d'application: IHC 1:30-1:150, ELISA 1:2000-1:10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1.2 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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. Avoid freeze / thaw cycles.

Détails sur COX17

Antigène: COX17 (COX17 Cytochrome C Oxidase Assembly Protein 17 (COX17))

Autre désignation: COX17

Sujet: Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be involved in the recruitment of copper to mitochondria for incorporation into the COX apoenzyme. This protein shares 92 % amino acid sequence identity with mouse and rat Cox17 proteins. This gene is no longer considered to be a candidate gene for COX deficiency. A pseudogene COX17P has been found on chromosome 13.

UniProt: Q14061