MT-ND6 anticorps

N° du produit ABIN7239227

Détail du produit anti-MT-ND6 anticorps

Antigène: MT-ND6 (Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MT-ND6 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Synthetic peptide of human MT-ND6

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.7 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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 MT-ND6

Antigène: MT-ND6 (Mitochondrially Encoded NADH Dehydrogenase 6 (MT-ND6))

Autre désignation: MT-ND6 (MT-ND6 Produits)

Synonymes: anticorps MTND6, anticorps NADH6, anticorps mitochondrial NADH-ubiquinone oxidoreductase chain 6, anticorps NADH dehydrogenase, subunit 6 (complex I), anticorps NADH dehydrogenase subunit 6, anticorps NADH dehydrogenasesubunit 6, anticorps mt:ND6, anticorps ND6, anticorps nad6

Sujet: NADH:ubiquinone oxidoreductase (complex I) is an extremely complicated multiprotein complex located in the inner mitochondrial membrane. Human complex I is important for energy metabolism because its main function is to transport electrons from NADH to ubiquinone, which is accompanied by translocation of protons from the mitochondrial matrix to the intermembrane space. Human complex I appears to consist of 41 subunits. A small number of complex I subunits are the products of mitochondrial genes (subunits 1-7), while the remainder are nuclear encoded and imported from the cytoplasm. The significance of NADH dehydrogenase subunit 6 (ND6) is rapidly becoming increasingly apparent as many mutations leading to amino acid changes in this subunit are associated with known mitochondrial diseases.

NCBI Accession: YP_003024037

UniProt: P03923