SURF1 anticorps (AA 27-295) (Cy3)

N° du produit ABIN8043900

L’anticorps anti-SURF1 Polyclonal Lapin est utilisé pour la détection de SURF1 dans des échantillons de Humain, Rat, Souris et Singe. Il a été validé pour FACS.

Aperçu rapide pour SURF1 anticorps (AA 27-295) (Cy3) (ABIN8043900)

Antigène: SURF1 (Surfeit 1 (SURF1))

Reactivité: Humain, Rat, Souris, Singe

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SURF1 est conjugé à/à la Cy3

Application: Flow Cytometry (FACS)

Détail du produit anti-SURF1 anticorps (Cy3)

Épitope: AA 27-295

Fonction: Anti-SURF1 Antibody Cy3 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human SURF1 recombinant protein (Position: S27-R295).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, 1-3 μg/1x10⁶ cells

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur SURF1

Antigène: SURF1 (Surfeit 1 (SURF1))

Autre désignation: SURF1

Sujet:

Background: Surfeit locus protein 1 (SURF1) is a protein that in humans is encoded by the SURF1 gene. 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 biional 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.

Gene Full Name: SURF1 cytochrome c oxidase assembly factor

ID gène: 6834

UniProt: Q15526

Pathways: Proton Transport, Ribonucleoside Biosynthetic Process