COX3 anticorps (AA 25-130) (Alexa Fluor 750)

N° du produit ABIN5000426

Détail du produit anti-COX3 anticorps (Alexa Fluor 750)

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

Épitope: AA 25-130

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp COX3 est conjugé à/à la Alexa Fluor 750

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

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: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

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:

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