

Product description
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 ra
Source
Rabbit
Applications
WB,ELISA
Reactivity
Human
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Storage
-20°C/1 year
Specificity
COX2 Polyclonal Antibody detects endogenous levels of protein.
Source/Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Immunogen
Synthesized peptide derived from human protein . at AA range: 40-120
Uniprot No
P00403
Form
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Clonality
Polyclonal
Background
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 ra
Other
Gene_name: MT-CO2 COII COXII MTCO2 ; Protein_name: Cytochrome c oxidase subunit 2 (Cytochrome c oxidase polypeptide II); Expression: Blood,Bone fossil,Bones,Breast cancer,Distant normal tissue,Endometrial ade
Mol.Wt (Da)
24 kD
Concentration
1 mg/ml
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