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Rabbit Anti-SCO2 Antibody (CSB-PA020853ESR2HU)
Supplier: CUSABIO BIOTECH CO.
Protein SCO2 homolog Antibody,mitochondrial Antibody,SCO2 AntibodyMore alternative names for the antibody
Cytochrome oxidase deficient homolog 2 antibody|MGC125823 antibody|MGC125825 antibody|OTTHUMP00000196774 antibody|OTTHUMP00000196775 antibody|Protein SCO2 homolog, mitochondrial antibody|SCO (cytochrome oxidase deficient, yeast) homolog 2 antibody|SCO 1L antibody|SCO 2 antibody|SCO cytochrome oxidase deficient homolog 2 (yeast) antibody|SCO cytochrome oxidase deficient homolog 2 antibody|SCO1L antibody|SCO2 antibody|SCO2_HUMAN antibody|Synthesis of cytochrome c oxidase 2 antibody
Anti-SCO2 antibody (ab115877)
Anti-SCO2 antibody (ab115877)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Protein SCO2 homolog, mitochondrial protein (1-130AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Protein function|| |
Acts as a copper chaperone, transporting copper to the Cu(A) site on the cytochrome c oxidase subunit II (COX2).
|Protein tissue specificity|| |
|Involvement in disease|| |
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 (CEMCOX1) [MIM:604377]: A disorder characterized by hypotonia, developmental delay, hypertrophic cardiomyopathy, lactic acidosis, gliosis, neuronal loss in basal ganglia, brainstem and spinal cord, and cytochrome c oxidase deficiency. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Myopia 6 (MYP6) [MIM:608908]: A refractive error of the eye, in which parallel rays from a distant object come to focus in front of the retina, vision being better for near objects than for far. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Leigh syndrome (LS) [MIM:256000]: An early-onset progressive neurodegenerative disorder characterized 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. Clinical features depend on which areas of the central nervous system are involved and include subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, and dysphagia. . Note=The disease may be caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the SCO1/2 family.
|Protein cellular localization|| |
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CUSABIO BIOTECH CO.
|Product type|| |
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