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Cytochrome c oxidase (COX) catalyzes the transfer of electrons from cytochrome c to molecular oxygen, which helps to maintain the proton gradient across the inner mitochondrial membrane that is necessary for aerobic ATP production. Additionally we are shipping SCO2 Proteins (11) and many more products for this protein.
Showing 10 out of 44 products:
Human Polyclonal SCO2 Primary Antibody for IHC, ELISA - ABIN1003127
Glerum, Shtanko, Tzagoloff: SCO1 and SCO2 act as high copy suppressors of a mitochondrial copper recruitment defect in Saccharomyces cerevisiae. in The Journal of biological chemistry 1996
Show all 4 references for ABIN1003127
Data suggest that physical exercise attenuates age-related changes in mitochondrial COX biogenesis and p53 activity targeting SCO2 and mitochondria, and thereby induces antisenescent and protective effects in cardiac muscle.
Results describe the tissue distribution of SCO1 and SCO2 in mouse and human tissues.
To understand the biological role of SCO2, mice harboring both a Sco2 knock-out (KO) allele and a Sco2 knock-in (KI) E129K allele, corresponding to the common E140K mutation in humans, were studied.
findings show that p53 modulates the balance between the utilization of respiratory and glycolytic pathways; identifed Synthesis of Cytochrome c Oxidase 2 (SCO2) as the downstream mediator of this effect
Geranylgeranoic acid increased the SCO2 gene expression, which might enhance aerobic respiration.
oncoprotein HBXIP (show HBXIP Antibodies) enhances glucose metabolism reprogramming through suppressing SCO2 and PDHA1 (show PDHA1 Antibodies) in breast cancer
Cooperation between COA6 and SCO2 in COX2 (show COX2 Antibodies) maturation during cytochrome c (show CYCS Antibodies) oxidase assembly links two mitochondrial cardiomyopathies.
Sco1 is a metallochaperone that selectively transfers Cu(I) ions based on loop recognition, whereas Sco2 is a copper-dependent thiol reductase of the cysteine ligands in the oxidase.
Letter/Case Report: SCO2 mutations resulting in Leigh disease revealed at autopsy.
mutation in LRPAP1 is associated with high myopia. Further studies are expected to evaluate the pathogenicity of the variants in CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2.
COX20 cooperates with SCO1 (show SCO1 Antibodies) and SCO2 to mature COX2 (show COX2 Antibodies) and promote the assembly of cytochrome c (show CYCS Antibodies) oxidase.
alpha-particle-induced bystander effect is regulated by p53 and its downstream SCO2 in the irradiated hepatoma cells
oroxylin A could increase protein and mRNA expression of TP53-induced glycolysis and apoptosis regulator (TIGAR (show C12orf5 Antibodies)) and synthesis of cytochrome c oxidase 2 (show COX2 Antibodies) (SCO2), which are the key metabolic modulators regulated by p53 (show TP53 Antibodies).
Autosomal recessive mutations in SCO2 are known to be associated with COX (show COX8A Antibodies) deficiency recognized as fatal infantile cardio-encephalomyopathy
Cytochrome c oxidase (COX) catalyzes the transfer of electrons from cytochrome c to molecular oxygen, which helps to maintain the proton gradient across the inner mitochondrial membrane that is necessary for aerobic ATP production. Human COX is a multimeric protein complex that requires several assembly factors\; this gene encodes one of the COX asembly factors. The encoded protein is a metallochaperone that is involved in the biogenesis of cytochrome c oxidase subunit II. Mutations in this gene are associated with fatal infantile encephalocardiomyopathy.
protein SCO2 homolog, mitochondrial
, SCO cytochrome oxidase deficient homolog 2
, cytochrome oxidase deficient homolog 2