Recombinatie MDAC2 monoklonaal antilichaam

Cofactor:Copper A., disease:Defects in MT-CO2 are a cause of cytochrome c oxidase deficiency (COX deficiency) [MIM:220110]; also called mitochondrial complex IV deficiency. COX deficiency is a clinically heterogeneous disorder. The clinical features are ranging from isolated myopathy to severe multisystem disease, with onset from infancy to adulthood., disease:Defects in MT-CO2 are associated with tumor formation., Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. Subunit 2 transfers the electrons from cytochrome c via its binuclear copper A center to the bimetallic center of the catalytic subunit 1., similarity:Belongs to the cytochrome c oxidase subunit 2 family.

MTCO2

P00403

Human

Recombinant Human MTCO2 rabbit protein

COX; Mtco; Cytochrome c oxidase subunit; MT-CO; MT CO; MT-CO2; COII; MTCO2; COX2; Cytochrome c oxidase II; Cytochrome c oxidase polypeptide II; Cytochrome c oxidase subunit 2; MT CO2; COXII; COX2; COX2; COXII; Cytochrome c oxidase II; MT-CO2; COII; COX2

10F7

Unconjugated

WB; IHC

Signal Transduction; Cancer; Metabolism

Protein A

0.2 mg/mL

IHC 1:200-1000; WB 1:1000-5000

PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Ice bag

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

https://789.bio/eb/aN4y8VJ2

26 kDa

21 kDa

IgG, κ