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Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Additionally we are shipping COX2 Antibodies (84) and and many more products for this protein.
Showing 10 out of 16 products:
Mouse (Murine) COX2 ELISA Kit for Sandwich ELISA - ABIN426443
Cherng, Tsai, Yu, Lin: Molecular mechanisms underlying chemopreventive activities of glycyrrhizic acid against UVB-radiation-induced carcinogenesis in SKH-1 hairless mouse epidermis. in Radiation research 2011
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Rat (Rattus) COX2 ELISA Kit for Competition ELISA - ABIN1052816
Sakthivel, Guruvayoorappan: Protective effect of Acacia ferruginea against ulcerative colitis via modulating inflammatory mediators, cytokine profile and NF-?B signal transduction pathways. in Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer 2014
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Tested the roles of COX-2 and EP receptors in VEGF-C (show VEGFC ELISA Kits) and -D production by a highly metastatic COX-2 expressing murine breast cancer cell line C3L5.
Rickettsia conorii infection of susceptible mice, therefore, results in selective regulation of the expression of HO-1 (show HMOX1 ELISA Kits) and COX-2 in a manner dependent on the target host tissue's cellular environment and the propensity of infection with rickettsiae.
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.
Cytochrome c oxidase subunit II is inactivated by mutant SOD1 (show SOD1 ELISA Kits) in motor neurons; this inactivation requires nitric oxide.
Data suggest that the binding of proteins such as cytochrome c oxidase subunit II to epidermal growth factor (show EGF ELISA Kits) receptors may positively regulate survival pathways that contribute to oncogenesis.
A lifetime absence of COX-2 produces multiple changes in brain lipid composition. These changes may be related to reported changes in fatty acid kinetics and in resistance to neuroinflammation and excitotoxicity in the COX-2(-/-) mouse
Activation of the signaling pathway is responsible for keratinocyte proliferation and reveal a positive feedback loop between COX-2 and PGE2.
The gene expression of Cox2 in adipocytes was studied.
co-ordinated post-translational modifications of p65 (show NFkBP65 ELISA Kits) and histone H3 (show HIST3H3 ELISA Kits) involving phosphorylation and acetylation drive COX-2-dependent transcriptional activation of the MMP-9 (show MMP9 ELISA Kits) gene in response to challenge of macrophages with M. avium.
aberrant renin (show REN ELISA Kits)-producing cells in Cx40 (show GJA5 ELISA Kits)-deficient kidneys express significant amounts of COX-2
Data indicate that the proton-pumping pathway of heart cytochrome c (show CYCS ELISA Kits) oxidase includes a hydrogen-bond network and a water channel (show AQP4 ELISA Kits) located in tandem between the positive and negative side of the mitochondrial membrane.
Study suggests that His503 is involved in the proton supply to the D-path as a proton acceptor in cytochrome c (show CYCS ELISA Kits) oxidase.
Data suggest that the axial Met residue moderately increased the redox potential of the Cu(A) site in cytochrome c (show CYCS ELISA Kits) oxidase.
Studies indicate that heart cytochrome c (show CYCS ELISA Kits) oxidase subunits I, II and III are encoded by the mitochondrial genome.
extensive pre- and intrapartal rise of COX (show COX7A1 ELISA Kits)-II expression in bovine placentomes with a 70-100-fold increase of COX (show COX7A1 ELISA Kits)-II-mRNA levels
B1 receptors are coupled to COX2 (show PTGS2 ELISA Kits) in causing endothelium-independent contractions in endotoxin-treated pig coronary arteries
Expression of COX-2 (show PTGS2 ELISA Kits) was strongest in gilts with acute endometritis, but did not differ between those with chronic endometritis and normal endometrium.
Pretreatment of cells with selective COX-2 blocker etodolac markedly inhibited ICl.
Safflower injection may attenuate lung ischemia/reperfusion injury through inhibiting cyclooxygenase-2 (show PTGS2 ELISA Kits) expression.
The RNA interference targeting COX-2 can effectively inhibit the expression of COX-2 and MMP-2 (show MMP2 ELISA Kits) in IL-1alpha stimulated rabbit corneal stromal cells in vitro.
The sequencing analysis revealed the presence of 17 variants, mostly causing non-synonymous changes in conserved amino acid residues, typically distributed in the MT-CO2 gene of MUTYH (show MUTYH ELISA Kits)-associated polyposis patients (P < 0.0001), who frequently carried the hot spot m.7763G>A variant.
Results find that COA6 associates with COX2 and is crucial for its maturation and complex IV biogenesis. Also, COA6 interacts with the copper chaperone SCO1 which indicates that COA6 is intrinsically involved in the copper delivery process for COX2.
Mutational analysis show a novel MTCO2 mutation 8249G>A pathogenic variation in Tunisian patients with mitochondrial myopathy.
We also detected in 4 asthenospermic patients a double novels mutations, the first was found in COXII gene (m.8021 G/A) that was absent in normospermic infertile men.
The presence of a non-synonymous variation in the COII strongly correlated with poor survival in patients with cytogenetically normal acute myeloid leukemia (show BCL11A ELISA Kits).
Protein modeling revealed loss of function mutations of ND6 (show MT-ND6 ELISA Kits) and COX (show COX8A ELISA Kits)-II proteins in malignant vs benign tumors
COX-2 expression played an essential role in the proliferation and metastasis of tongue cancer.
Novel COII mutations responsible for maternally inherited nonsyndromic hearing loss
The apoptotic index of pulmonary vascular endothelial cells was negatively correlated with COXII expression in patients with chronic obstructive pulmonary disease.
COX (show COX8A ELISA Kits)-II is induced in HIV infected apoptotic T-cells.
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. Subunit 2 transfers the electrons from cytochrome c via its binuclear copper A center to the bimetallic center of the catalytic subunit 1.
cytochrome c oxidase subunit II
, cytochrome c oxidase subunit ii
, cytochrome C oxidase subunit II
, PGH synthase 2
, PHS II
, cyclooxygenase 2
, prostaglandin G/H synthase 2
, prostaglandin H2 synthase 2