MT-ND5 anticorps (AA 154-570)

N° du produit ABIN7871002

Cet anticorps anti-MT-ND5 Polyclonal Lapin (ABIN7871002) détecte spécifiquement MT-ND5 dans WB, ELISA, FACS, IHC (p) et IF. L’anticorps est réactif avec des échantillons de Humain et Rat.

Aperçu rapide pour MT-ND5 anticorps (AA 154-570) (ABIN7871002)

Antigène: MT-ND5 (Mitochondrially Encoded NADH Dehydrogenase 5 (MT-ND5))

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MT-ND5 est non-conjugé

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

Détail du produit anti-MT-ND5 anticorps

Épitope: AA 154-570

Fonction: MT-ND5 Antibody / NADH-ubiquinone oxidoreductase chain 5

Purification: Antigen affinity purified

Immunogène: Recombinant human protein (amino acids L154-Q570) was used as the immunogen for the MT-ND5 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the MT-ND5 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the MT-ND5 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur MT-ND5

Antigène: MT-ND5 (Mitochondrially Encoded NADH Dehydrogenase 5 (MT-ND5))

Autre désignation: MT-ND5

Sujet: MT-ND5 is a gene of the mitochondrial genome coding for the NADH-ubiquinone oxidoreductase chain 5 protein (ND5). 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. NADH dehydrogenase subunit 5 (ND5) is most likely a component of the hydrophobic protein fragment of Complex I. Mutations in the gene encoding for ND5 are implicated in Mitochondrial neurogastrointestinal encephalomyopathy, an autosomal recessive multisystem disorder that results in dramatically elevated levels of circulating thymidine and deoxyuridine.

UniProt: P03915