SKU: WP11765 Categories: ,

COX15 Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP11765-100
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Product details

Background:

Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be essential for the biogenesis of COX formation and may function in the hydroxylation of heme O, according to the yeast mutant studies. This protein is predicted to contain 5 transmembrane domains localized in the mitochondrial inner membrane. Alternative splicing of this gene generates two transcript variants diverging

Specifications

Size50μL/100μL
TargetCOX15
ReactivityHuman, Mouse, Rat
ApplicationsIHC, IF, ELISA
MW(Calculated)46kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:100-1:300; ELISA 1:5000; IF 1:50-200 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenThe antiserum was produced against synthesized peptide derived from human COX15. AA range:181-230
SpecificityCOX15 Polyclonal Antibody detects endogenous levels of COX15 protein.
Gene NameCOX15
Protein NameCytochrome c oxidase assembly protein COX15 homolog
Other NameCOX15; / Cytochrome c oxidase assembly protein COX15 homolog
SpeciesHuman
Gene ID1355
UniprotQ7KZN9,
Species.1Mouse
Gene ID.1226139
Uniprot.1Q8BJ03
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationMitochondrion membrane; Multi-pass membrane protein .
Tissue ExpressionPredominantly found in tissues characterized by high rates of oxidative phosphorylation (OxPhos), including muscle, heart, and brain.
Signaling_pathway
Research Areas>>Oxidative phosphorylation; / >>Porphyrin metabolism; / >>Metabolic pathways; / >>Biosynthesis of cofactors; / >>Thermogenesis
FunctionDisease:Defects in COX15 are a cause of cytochrome c oxidase deficiency (COX deficiency) [MIM:220110]. COX deficiency is a clinically heterogeneous disorder. The clinical features range from isolated myopathy to severe multisystem disease with onset from infancy to adulthood.,Disease:Defects in COX15 are a cause of Leigh syndrome [MIM:256000]. Leigh syndrome is an early-onset progressive neurodegenerative disorder characterized by delayed onset of symptoms, hypotonia, feeding difficulties, failure to thrive, motor regression and brainstem signs. Diagnosis is confirmed by the presence of focal, bilateral lesions in one or more areas of the central nervous system including the brainstem, thalamus, basal ganglia, cerebellum and spinal cord.,Function:May be involved in the biosynthesis of heme A.,pathway:Porphyrin metabolism; heme A biosynthesis; heme A from heme O: step 1/1.,similarity:Belongs to the COX15/ctaA family.,tissue specificity:Predominantly found in tissues characterized by high rates of oxidative phosphorylation (OxPhos), including muscle, heart, and brain.,
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