COX3 anticorps (AA 25-130) (Biotin)

N° du produit ABIN751365

Cet anticorps anti-COX3 est un anticorps Lapin Polyclonal détectant COX3 dans WB, ELISA, IHC (fro) et IHC (p). Adapté pour Souris et Rat.

Aperçu rapide pour COX3 anticorps (AA 25-130) (Biotin) (ABIN751365)

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

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp COX3 est conjugé à/à la Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-COX3 anticorps (Biotin)

Épitope: AA 25-130

Réactivité croisée: Souris, Rat

Homologie: Human,Dog,Cow,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human COX3

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur COX3

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

Autre désignation: COX3

Sujet:

Synonyms: Cytochrome c oxidase polypeptide III, Cytochrome c oxidase subunit 3, COIII, COX3, COX-3, COXIII, MT CO3, MTCO3, COX3_HUMAN.

Background: Cytochrome C Oxidase subunits I, II and III form the functional core of the enzyme complex.Defects in Cytochrome C Oxidase subunits III are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in Cytochrome C Oxidase subunits III are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.

ID gène: 4514