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GPX1 encodes a member of the glutathione peroxidase family. Additionally we are shipping Glutathione Peroxidase 1 Antibodies (162) and Glutathione Peroxidase 1 Proteins (18) and many more products for this protein.
Showing 10 out of 81 products:
Human Glutathione Peroxidase 1 ELISA Kit for Sandwich ELISA - ABIN414656
Nalkiran, Turan, Arikan, Kahraman, Acar, Yaylim, Ergen: Determination of gene expression and serum levels of MnSOD and GPX1 in colorectal cancer. in Anticancer research 2014
Show all 2 references for ABIN414656
Rat (Rattus) Glutathione Peroxidase 1 ELISA Kit for Sandwich ELISA - ABIN416232
Rodrigues, Bergamaschi, Fernandes, Paredes-Gamero, Curi, Ferreira, Araujo, Punaro, Maciel, Nogueira, Higa: P2×(7) receptor in the kidneys of diabetic rats submitted to aerobic training or to N-acetylcysteine supplementation. in PLoS ONE 2014
Show all 2 references for ABIN416232
GPX1*Pro198Leu AND GPX3 (show GPX3 ELISA Kits) rs2070593 as genetic risk markers for Italian asthmatic patients
An increase in both SOD1 (show SOD1 ELISA Kits) and GPx1 activity is involved in the protective effect of sulodexide on ischemic endothelial cells.
In patients with chronic hepatitis C, the GPX1 Pro198Leu polymorphism, alone or combined with the CAT C-262T, was associated with high risk of fibrosis severity and hepatocellular carcinoma (HCC (show FAM126A ELISA Kits)). In addition, GPX1 polymorphism was also associated with advanced stages of HCC (show FAM126A ELISA Kits).
No significant difference was found for NRAMP1 (show SLC11A1 ELISA Kits) and hGPX1 gene polymorphisms associated with recurrence time.
Experimental and clinical data support a role for GPx-1 in the pathogenesis of inflammatory bowel disease (IBD), authors propose that GPX1 is the most relevant gene within IBD locus 12.
Findings demonstrated that miR (show MLXIP ELISA Kits)-153 overexpression decreased radioresistance and stemness of GSCs through targeting Nrf-2 (show GABPA ELISA Kits)/GPx1/ROS (show ROS1 ELISA Kits) pathway.
Pro198Leu and OGG1 (show OGG1 ELISA Kits) Ser326Cys polymorphisms were not associated with panic disorder (PD) risk in Turkish patients; however, a gender-specific effect of GPX1 Pro198Leu C allele may be associated with PD development
GPX1 polymorphism may be an important factor modifying oxidative stress response in breast cancer subjects.
GPx1 rs1800668 polymorphism does not play a major role in sensitivity-related illnesses -related oxidative stress development.
The minor T-allele of rs3448 of GPX1 was associated with kidney complications (incidences of microalbuminuria, renal events and ESRD) in patients with type 1 diabetes.
Plasmalogen enrichment via batyl alcohol supplementation attenuated atherosclerosis in ApoE (show APOE ELISA Kits)- and ApoE (show APOE ELISA Kits)/GPx1-deficient mice.
Gpx1 expression in the mouse skeletal muscle can be altered by both exercise and dyslipidemia through changes in DNA methylation (show HELLS ELISA Kits), leading to a fine regulation of free radical metabolism.
our findings unveil a new metabolic role for Reg3beta in protein nitration and a new biosynthesis control of GPX1 by a completely "unrelated" regenerating protein, Reg3beta, via transcriptional activation of Scly (show SCLY ELISA Kits)
Rora (show RORA ELISA Kits) induces the mRNA level of antioxidant enzymes, superoxide dismutase 2 (show SOD2 ELISA Kits) and glutathione peroxidase 1, through the Rora (show RORA ELISA Kits) response elements located in the upstream promoters of Sod2 (show SOD2 ELISA Kits) and Gpx1.
High-fat-fed Gpx1(-/-) mice also exhibited decreased hepatic steatosis and liver damage accompanied by decreased plasma insulin (show INS ELISA Kits) and decreased glucose-induced insulin (show INS ELISA Kits) secretion.
we propose that ileocolitis in the DKO mice is caused by Nox1 (show NOX1 ELISA Kits), which is induced by TNF (show TNF ELISA Kits). The milder disease in female het-TKO (show MRPS12 ELISA Kits) intestine is probably due to random or imprinted X-chromosome inactivation, which produces mosaic Nox1 (show NOX1 ELISA Kits) expression.
PD-linked mutations in Parkin (show PARK2 ELISA Kits) and DJ-1 (show PARK7 ELISA Kits) cause dysregulation of neurotransmitter systems beyond the nigrostriatal dopaminergic circuit especially in the context of Gpx1 deficiency.
During early differentiation of embryonic stem (ES) cells, the quick degradation of GPx-1 was mediated by proteasome. Both knockdown of GPx-1 expression with shRNA and inhibiting GPx-1 activity by inhibitor led to the differentiation of ES cells.
Data indicate that he macrophage-colony-stimulating factor (show CSF2 ELISA Kits) (MCSF (show CSF1 ELISA Kits)) and oxLDL-induced proliferation of peritoneal macrophages from GPx-1(-/-)ApoE (show APOE ELISA Kits)(-/-) mice was mediated by the ERK1/2 (show MAPK1/3 ELISA Kits) (extracellular-signal regulated kinase 1/2 (show MAPK3 ELISA Kits)) signaling pathway.
The present study has sought to investigate the extent of vascular dysfunction and oxidant formation in glutathione peroxidase-1-deficient (GPx-1(-/-)) mice during the aging process with special emphasis on dysregulation of the endothelial NO synthase (show NOS ELISA Kits).
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.
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
, putative glutathione peroxidase
, glutathione peroxidase 1
, cellular glutathione peroxidase
, selenium-dependent glutathione peroxidase 1
, cytosolic glutathione peroxidase