Thermo Fisher Scientific COX3 Monoclonal Antibody (DA5BC4)

Applications

Tested Dilution

Publications

Western Blot (WB)

2-4 µg/mL

View 4 publications 4 publications

Product Specifications

Species Reactivity

Human, Mouse, Rat, Yeast

Published species

Yeast

Host/Isotype

Mouse / IgG2a, kappa

Class

Monoclonal

Type

Antibody

Clone

DA5BC4

Immunogen

Full length native Yeast Cytochrome C Oxidase subunit III if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:COX3,uniProtId:P00420-1,ncbiNodeId:-23,antigenRange:1-269,antigenLength:269,antigenImageFileName:459300_COX3_P00420-1_House_mouse.svg,antigenImageFileNamePDP:459300_COX3_P00420-1_House_mouse_PDP.jpeg,sortOrder:3}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

IgG fraction

Storage buffer

HEPES buffered saline

Contains

0.02% sodium azide

Storage conditions

4° C, do not freeze

Shipping conditions

Wet ice

RRID

AB_10374345

Product Specific Information

Positive control: Isolated mitochondria from Human , Rat and Mouse hearts.

WB Predicted molecular weight: 30 kDa.

Target Information

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.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.