SCO2 anticorps (AA 1-130)

N° du produit ABIN6147457

Détail du produit anti-SCO2 anticorps

Antigène: SCO2 (SCO2 Cytochrome C Oxidase Assembly Protein (SCO2))

Épitope: AA 1-130

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SCO2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Séquence: MLLLTRSPTA WHRLSQLKPR VLPGTLGGQA LHLRSWLLSR QGPAETGGQG QPQGPGLRTR LLITGLFGAG LGGAWLALRA EKERLQQQKR TEALRQAAVG QGDFHLLDHR GRARCKADFR GQWVLMYFGF

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-130 of human SCO2 (NP_001162582.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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 SCO2

Antigène: SCO2 (SCO2 Cytochrome C Oxidase Assembly Protein (SCO2))

Autre désignation: SCO2 (SCO2 Produits)

Synonymes: anticorps CEMCOX1, anticorps MYP6, anticorps SCO1L, anticorps SCO cytochrome oxidase deficient homolog 2 (yeast), anticorps SCO2 cytochrome c oxidase assembly protein, anticorps SCO2, cytochrome c oxidase assembly protein, anticorps SCO2, anticorps Sco2

Sujet: Cytochrome c oxidase (COX) catalyzes the transfer of electrons from cytochrome c to molecular oxygen, which helps to maintain the proton gradient across the inner mitochondrial membrane that is necessary for aerobic ATP production. Human COX is a multimeric protein complex that requires several assembly factors, this gene encodes one of the COX assembly factors. The encoded protein is a metallochaperone that is involved in the biogenesis of cytochrome c oxidase subunit II. Mutations in this gene are associated with fatal infantile encephalocardiomyopathy and myopia 6.,SCO2,CEMCOX1,MYP6,SCO1L,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Oxidative phosphorylation,SCO2

Poids moléculaire: 29 kDa

ID gène: 9997

UniProt: O43819

Pathways: Transition Metal Ion Homeostasis, L'effet Warburg