SURF1 anticorps

N° du produit ABIN7256170

Détail du produit anti-SURF1 anticorps

Antigène: SURF1 (Surfeit 1 (SURF1))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SURF1 est non-conjugé

Application: Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human SURF1 (NP_003163.1).

Isotype: IgG

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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 SURF1

Antigène: SURF1 (Surfeit 1 (SURF1))

Autre désignation: SURF1 (SURF1 Produits)

Synonymes: anticorps BcDNA:GH23574, anticorps CG9943, anticorps Dmel\\CG9943, anticorps GB14201, anticorps SURF1, anticorps im:6898613, anticorps zgc:158646, anticorps Ab1-205, anticorps SURF-1, anticorps 0610010F23Rik, anticorps Surf-1, anticorps SURFEIT 1, anticorps Surfeit 1, anticorps surfeit locus protein 1, anticorps SURF1, cytochrome c oxidase assembly factor, anticorps surfeit 1, anticorps surfeit gene 1, anticorps Surfeit locus 1 cytochrome c oxidase biogenesis protein, anticorps Surf1, anticorps LOC413781, anticorps SURF1, anticorps surf1

Sujet: This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency.

ID gène: 6834

UniProt: Q15526

Pathways: Proton Transport, Ribonucleoside Biosynthetic Process