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GPX1 encodes a member of the glutathione peroxidase family. Additionally we are shipping Glutathione Peroxidase 1 Antibodies (163) and Glutathione Peroxidase 1 Kits (65) and many more products for this protein.
Showing 10 out of 18 products:
This meta-analysis showed a significant association between low GPx level and vitiligo (show MITF Proteins).
GPx-1 Pro200Leu polymorphism was associated with obesity especially with morbid obesity, but not with obese participants with prediabetes or diabetes
variants of GPx1 and MnSOD (show SOD2 Proteins) should not be considered as a risk factor of laryngeal squamous cell carcinoma.
Glucose oscillations may exert more deleterious effects on the endothelium than high glucose, likely due to an impaired response of glutathione peroxidase-1, coupled by the upregulation of miR (show MLXIP Proteins)-185
Results showed no statistically significant difference between the vitiligo (show MITF Proteins) and MnSOD (show SOD2 Proteins) Ala-9Val and GPx1 Pro198Leu gene polymorphisms in Turkish population.
The purpose of the study was to evaluate the plasma level of superoxide dismutase (SOD (show SOD1 Proteins)), catalase (show CAT Proteins) (CAT), and glutathione peroxidase (GPX) and the association between polymorphic variants in genes encoding for GPx1, SOD (show SOD1 Proteins), CAT and the risk of distal symmetric polyneuropathy in type 2 diabetes mellitus patients.
This study examined the relationship between levels of GPx activity, reactive oxygen species, and platelet activation in 51 acute coronary syndrome (ACS) patients.
The MnSOD (show SOD2 Proteins), GPX1 and CAT genotypes and allele frequencies of acute kidney injury patients did not differ significantly from those of healthy controls.
the presence of variant allele and genotype of GPX1 Pro198Leu and GSTP1 (show GSTP1 Proteins) Ile105Val gene polymorphisms may modulate the risk of developing acute myeloid leukemia (show BCL11A Proteins)
GPX1 Pro198Leu rs1050450 genotypes differentially affect the selenium status and GPx activity.
Exposure to far infrared rays significantly protects acute restraint stress oxidative burdens via inhibition of JAK2 (show JAK2 Proteins)/STAT3 (show STAT3 Proteins) signaling by induction of GPx-1.
Genetic inhibition of Gpx1 potentiates cocaine-induced renal damage via activation of AT1R (show AGTRAP Proteins) by inhibition of PI3K-Akt (show AKT1 Proteins) 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 (show APOE Proteins)- and ApoE (show APOE Proteins)/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 Proteins), 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 Proteins)
Rora (show RORA Proteins) induces the mRNA level of antioxidant enzymes, superoxide dismutase 2 (show SOD2 Proteins) and glutathione peroxidase 1, through the Rora (show RORA Proteins) response elements located in the upstream promoters of Sod2 (show SOD2 Proteins) and Gpx1.
High-fat-fed Gpx1(-/-) mice also exhibited decreased hepatic steatosis and liver damage accompanied by decreased plasma insulin (show INS Proteins) and decreased glucose-induced insulin (show INS Proteins) secretion.
we propose that ileocolitis in the DKO mice is caused by Nox1 (show NOX1 Proteins), which is induced by TNF (show TNF Proteins). The milder disease in female het-TKO (show MRPS12 Proteins) intestine is probably due to random or imprinted X-chromosome inactivation, which produces mosaic Nox1 (show NOX1 Proteins) expression.
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