SURF1 anticorps (N-Term)

N° du produit ABIN2788832

L’anticorps Lapin Polyclonal anti-SURF1 a été validé pour WB. Il convient pour détecter SURF1 dans des échantillons de Humain, Boeuf (Vache), Cobaye et Cheval.

Aperçu rapide pour SURF1 anticorps (N-Term) (ABIN2788832)

Antigène: SURF1 (Surfeit 1 (SURF1))

Reactivité: Humain, Boeuf (Vache), Cobaye, Cheval

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SURF1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SURF1 anticorps

Épitope: N-Term

Séquence: GLRAAGLGRA PASAAWRSVL RVSPRPGVAW RPSRCGSSAA EASATKAEDD

Homologie: Cow: 79%, Guinea Pig: 86%, Horse: 86%, Human: 100%

Attributs du produit: This is a rabbit polyclonal antibody against SURF1. It was validated on Western Blot.

Purification: Affinity Purified

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 300 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur SURF1

Antigène: SURF1 (Surfeit 1 (SURF1))

Autre désignation: 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.
Alias Symbols: -
Protein Interaction Partner: UBC, PTGES3, CHCHD4, SFXN3, NDUFA12, NDUFAF3, SAMM50, FKBP8, UQCRC1, SRSF5, ABCD3, NDUFV2, NDUFS8, NDUFS3, NDUFB8, ABCC1, CYC1, COX15,
Protein Size: 300

Poids moléculaire: 33 kDa

ID gène: 6834

NCBI Accession: NM_003172, NP_003163

UniProt: Q15526

Pathways: Proton Transport, Ribonucleoside Biosynthetic Process