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a dependence of COX1 AND capital ES, CyrillicOX2 expression on the presence of MMP-9 (show MMP9 ELISA Kits) was shown in neutrophil infiltration during inflammation.
CCOI expression is inhibited by osteopontin (show SPP1 ELISA Kits) as the result of a novel CD44 (show CD44 ELISA Kits)-dependent transcriptional regulatory mechanism of the mitochondrial H strand
The gene expression of Cox1 in adipocytes was studied.
CcOX (show COX5A ELISA Kits) I protein levels significantly decreased following CO exposure while enzyme turnover number and CcOX (show COX5A ELISA Kits) I mRNA levels remained unchanged.
IOP elevation may directly damage mitochondria in the ONH axons by promoting reduction of COX (show CPOX ELISA Kits), mitochondrial fission and cristae depletion, alterations of OPA1 (show MED12 ELISA Kits) and Dnm1 (show DNM1 ELISA Kits) expression, and induction of OPA1 (show MED12 ELISA Kits) release.
Tumor necrosis factor alpha (show TNF ELISA Kits) inhibits oxidative phosphorylation through tyrosine phosphorylation at subunit I of cytochrome c (show CYCS ELISA Kits) oxidase
patients with primary ovarian insufficiency exhibit an increased incidence of mitochondrial cytochrome c oxidase 1 gene mutations;MT-CO1 gene mutation may be causal in the disease
studies have provided mechanistic insights into crosstalk between assembly intermediates, import processes and the synthesis of COX (show COX8A ELISA Kits) subunits in mitochondria, thus linking conceptually separated functions.
The m.9267G>C MT-COIII mutation was present with a nonsynonymous inherited mitochondrial homoplasmic variation MT-COI m.5913 G>A.
A novel heteroplasmic mutation was identified in MTCO1, m.7402delC, causing frameshift and a premature termination codon in a mitochondrial encephalomyopathy patient with cytochrome c (show CYCS ELISA Kits) oxidase deficiency.
mitochondrial DNA mutations in COI resulting in increased reactive oxygen and reactive nitrogen generation may be involved in prostate cancer biology
Possible association of a novel missense mutation A6375G in the mitochondrial cytochrome C oxidase I gene with asthenospermia in the Tunisian population
Abeta (show APP ELISA Kits) 1-42 bound to a peptide comprising the amino-terminal region of cytochrome c oxidase subunit 1
Both full-length and truncated COX1 proteins physically interact with AFG3L2 (show AFG3L2 ELISA Kits).
Data show that homoplasmic G6709A (MT-CO1) and G14804A (MT-CYB (show MT-CYB ELISA Kits)) alterations cause amino acid changes in the highly conserved residues.
Screening of a Greek deafness population for the A7445G mitochondrial DNA COI mutation.
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. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B.
cytochrome c oxidase subunit I
, PGH synthase 1
, PHS 1
, cyclooxygenase 1
, cyclooxygenase 3
, prostaglandin G/H synthase 1
, prostaglandin G/H synthase and cyclooxygenase
, prostaglandin H2 synthase 1