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anti-Mouse (Murine) Glutathione Peroxidase 1 Antikörper:
anti-Human Glutathione Peroxidase 1 Antikörper:
anti-Rat (Rattus) Glutathione Peroxidase 1 Antikörper:
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Human Polyclonal Glutathione Peroxidase 1 Primary Antibody für IF (p), IHC (p) - ABIN750583
Miyamoto, Tsumuraya, Ohtaki, Dohi, Satoh, Xu, Tanaka, Murai, Watanabe, Sugiyama, Aruga, Shioda: PACAP38 Suppresses Cortical Damage in Mice with Traumatic Brain Injury by Enhancing Antioxidant Activity. in Journal of molecular neuroscience : MN 2014
Show all 3 Pubmed References
Mouse (Murine) Polyclonal Glutathione Peroxidase 1 Primary Antibody für ELISA, WB - ABIN4314701
Lubos, Kelly, Oldebeken, Leopold, Zhang, Loscalzo, Handy: Glutathione peroxidase-1 deficiency augments proinflammatory cytokine-induced redox signaling and human endothelial cell activation. in The Journal of biological chemistry 2011
Human Polyclonal Glutathione Peroxidase 1 Primary Antibody für ICC, IF - ABIN4314702
Bachmann, Burté, Pramana, Conte, Brown, Orimadegun, Ajetunmobi, Afolabi, Akinkunmi, Omokhodion, Akinbami, Shokunbi, Kampf, Pawitan, Uhlén, Sodeinde, Schwenk, Wahlgren, Fernandez-Reyes, Nilsson: Affinity proteomics reveals elevated muscle proteins in plasma of children with cerebral malaria. in PLoS pathogens 2014
Human Polyclonal Glutathione Peroxidase 1 Primary Antibody für IHC (p), IHC - ABIN251496
Kato, Kato, Abe, Matsumura, Nishino, Aoki, Itoyama, Asayama, Awaya, Hirano, Ohama et al.: Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ... in Acta neuropathologica 2005
Human Polyclonal Glutathione Peroxidase 1 Primary Antibody für ICC, IF - ABIN443480
Sun, Zhang, Zhong, Sun, Zhou: Dietary Fisetin Supplementation Protects Against Alcohol-Induced Liver Injury in Mice. in Alcoholism, clinical and experimental research 2016
Studied the importance of selenium in bovine female reproductive function. Gene expression analysis revealed selenoprotein gene GPX1 was significantly up-regulated in large healthy follicles.
did not find any significant inhibition of bovine GPx-1 by (S)- or (R)-misonidazole.
Data indicate mRNA level and activity of GPx1 are regulated by level of selenium supplied to hepatocytes.
homocysteine decreases GPx1 activity by altering the translational mechanism
glutathione peroxidase-1 activity is decreased by aminoglycosides through interference with selenocysteine incorporation
GPx1 plays a key role in blocking the promotion of porcine circovirus type 2 replication
The developmental expression of GPX1 and thioredoxin reductase during fetal development and the effect of maternal selenium consumption on the expression of these proteins are reported.
Notably, CUEDC2 (zeige CUEDC2 Antikörper) promoted E3 ubiquitin ligases tripartite motif-containing 33 (TRIM33 (zeige TRIM33 Antikörper))-mediated the antioxidant enzyme, glutathione peroxidase 1 (GPX1) ubiquitination, and proteasome-dependent degradation.
GPx1 does not clearly exacerbate hyperoxia-induced increases in oxidative stress or lung injury but may alter pulmonary immune function.
GPx-1 expression deters the unfolded protein response following exposure to cigarette smoke
Glutathione peroxidase 1 (GPx1) knockdown not only induced oxidative stress characterized by the increased production of reactive oxygen species (ROS (zeige ROS1 Antikörper)) but also caused reductive stress indicated by an elevation of glutathione (GSH)/oxidized GSH (GSSG) ratio.
Exposure to far infrared rays significantly protects acute restraint stress oxidative burdens via inhibition of JAK2 (zeige JAK2 Antikörper)/STAT3 (zeige STAT3 Antikörper) signaling by induction of GPx-1.
Genetic inhibition of Gpx1 potentiates cocaine-induced renal damage via activation of AT1R (zeige AGTRAP Antikörper) by inhibition of PI3K-Akt (zeige AKT1 Antikörper) signaling.
Glutathione peroxidase 1 deficiency attenuates concanavalin A-induced liver injury by induction of T-cell hyporesponsiveness through chronic reactive oxygen species exposure.
GPx1 was found to play a critical role in regulating pro-inflammatory pathways in vascular endothelium.
Plasmalogen enrichment via batyl alcohol supplementation attenuated atherosclerosis in ApoE (zeige APOE Antikörper)- and ApoE (zeige APOE Antikörper)/GPx1-deficient mice.
Gpx1 expression in the mouse skeletal muscle can be altered by both exercise and dyslipidemia through changes in DNA methylation (zeige HELLS Antikörper), leading to a fine regulation of free radical metabolism.
High GPX1 expression is associated with oral squamous cell carcinoma.
GPX1 is a gatekeeper restraining the oncogenic power of mitochondrial ROS (zeige ROS1 Antikörper) generated by SOD2 (zeige SOD2 Antikörper) is presented. Review.
Using lens epithelial cells derived from targeted inactivation of Prdx6 (zeige PRDX6 Antikörper)(-/-) gene and relative enzymatic and stability assays, we discovered dramatic increases in GSH-peroxidase (30%) and aiPLA2 (zeige PRDX6 Antikörper) (37%) activities and stability in the K122/142 R mutant, suggesting Sumo1 (zeige SUMO1 Antikörper) destabilized Prdx6 (zeige PRDX6 Antikörper) integrity
Coronary angiography findings indicated that individuals possessing Pro198Leu (CT) polymorphism were found to be associated with low erythrocyte GPX-1 activity and increased susceptibility for coronary artery disease.
High GPX1 expression is associated with Thyroid Tumors.
Data suggest that serum myeloperoxidase (zeige MPO Antikörper) (GPX1) levels are significantly associated with higher asymmetric dimethyl-arginine (ADMA) levels and up-regulation of circulating components of renin (zeige REN Antikörper)-angiotensin-aldosterone-system in patients with cardiovascular disease (CVD). Serum levels of ADMA and angiotensin II are more predictive for all-cause and CVD mortality compared to GPX1.
Pro198Leu of GPX1 might be a genetic risk factor in the development of Nephrolithiasis in South Iranian patients with lower Glutathione Peroxidase enzyme activity.
our data suggest that gene polymorphisms of GPX1 Pro198Leu and CAT C262T may have a protective role in the development of primary open-angle glaucoma in a Polish population.
Knockdown of GPX1 in hucMSCs abrogated antioxidant and anti-apoptotic abilities of hucMSC-Ex and diminished the hepatoprotective effects of hucMSC-Ex in vitro and in vivo. Thus, hucMSC-Ex promote the recovery of hepatic oxidant injury through the delivery of GPX1.
This gene encodes a member of the glutathione peroxidase family. Glutathione peroxidase functions in the detoxification of hydrogen peroxide, and is one of the most important antioxidant enzymes in humans. This protein is one of only a few proteins known in higher vertebrates to contain selenocysteine, which occurs at the active site of glutathione peroxidase and is coded by UGA, that normally functions as a translation termination codon. In addition, this protein is characterized in a polyalanine sequence polymorphism in the N-terminal region, which includes three alleles with five, six or seven alanine (ALA) repeats in this sequence. The allele with five ALA repeats is significantly associated with breast cancer risk. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
glutathione peroxidase Gpx1
, glutathione peroxidase
, cellular glutathione peroxidase
, cytosolic glutathione peroxidase
, putative glutathione peroxidase
, selenium-dependent glutathione peroxidase 1
, glutathione peroxidase 1
, glutathione peroxidase 1 S homeolog