COX3 anticorps (C-Term)

N° du produit ABIN2784116

Détail du produit anti-COX3 anticorps

Antigène: COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))

Épitope: C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp COX3 est non-conjugé

Application: Western Blotting (WB)

Séquence: FESPFTISDG IYGSTFFVAT GFHGLHVIIG STFLTICFIR QLMFHFTSKH

Homologie: Human: 100%

Attributs du produit: This is a rabbit polyclonal antibody against COX3. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the C terminal region of human COX3

Information d'application

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

Commentaires:

Antigen size: 260 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 COX3

Antigène: COX3 (COX-3) (Cytochrome C Oxidase Subunit 3 (COX-3))

Autre désignation: COX3 (COX-3 Produits)

Synonymes: anticorps COIII, anticorps MTCO3, anticorps cytochrome c oxidase III, anticorps cytochrome c oxidase subunit III, anticorps cytochrome c oxidase subunit 3, anticorps cytochrome oxidasesubunit 3, anticorps COX3, anticorps cox3

Sujet: COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.
Alias Symbols: MTCO3, COIII
Protein Interaction Partner: RAC1, LIG4, Htt, SNCA,
Protein Size: 260

Poids moléculaire: 29 kDa

ID gène: 4514

NCBI Accession: NP_536849

UniProt: P00414