SURF1 antibody

Catalog No. ABIN7256170

Product Details anti-SURF1 Antibody

Target: SURF1 (Surfeit 1 (SURF1))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SURF1 antibody is un-conjugated

Application: Immunohistochemistry (IHC)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

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

Isotype: IgG

Application Details

Application Notes: IHC 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for SURF1

Target: SURF1 (Surfeit 1 (SURF1))

Alternative Name: SURF1 (SURF1 Products)

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

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.

Gene ID: 6834

UniProt: Q15526

Pathways: Proton Transport, Ribonucleoside Biosynthetic Process