SURF1 anticorps

N° du produit ABIN7469040

Cet anticorps Lapin Polyclonal détecte spécifiquement SURF1 dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour SURF1 anticorps (ABIN7469040)

Antigène: SURF1 (Surfeit 1 (SURF1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SURF1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SURF1 anticorps

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human SURF1. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: Jurkat

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.83 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur SURF1

Antigène: SURF1 (Surfeit 1 (SURF1))

Autre désignation: SURF1 cytochrome c oxidase assembly factor

Sujet:

Synonyms: SURF1 cytochrome c oxidase assembly factor , CMT4K

Background: 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. [provided by RefSeq]

Poids moléculaire: 33 kDa

ID gène: 6834

UniProt: Q15526

Pathways: Proton Transport, Ribonucleoside Biosynthetic Process