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Glutathione peroxidase catalyzes the reduction of hydrogen peroxide, organic hydroperoxide, and lipid peroxides by reduced glutathione and functions in the protection of cells against oxidative damage. Additionally we are shipping GPX4 Antibodies (93) and GPX4 Kits (7) and many more products for this protein.
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We found that the gpx4b gene shows maternal and zygotic gene expression in the embryo proper compared to gpx4a that showed zygotic gene expression in the periderm covering the yolk cell only.
use GPX4 and GPX7 (show GPX7 Proteins) as possible markers for improving HCC (show FAM126A Proteins) diagnosis/prognosis.
One SNP (rs3746162) in GPX4 was significantly associated with bladder cancer recurrence after transurethral resection.
Hepatitis C virus (HCV) induces oxidative stress but controls it tightly by inducing ROS (show ROS1 Proteins) scavengers. Among these, GPx4 plays an essential role in the HCV life cycle.
GPX1 (show GPX1 Proteins), GPX3 (show GPX3 Proteins), and GPX4 genes may play a role in clear cell renal cell carcinoma (show MOK Proteins) cancerogenesis.
polymorphism of gene of glutathione peroxidase (show GPX1 Proteins) predisposes to more severe affection of liver and progression of chronic hepatitis C.
GPx4 is essential for maintaining oxidative homeostasis and keeping defense against oxidative stress in conjunctival epithelial cells.
Identification of truncating mutations in GPX4 in two families affected with Sedaghatian-type spondylometaphyseal dysplasia.
A membrane glycoprotein (show CD86 Proteins) GPX4 was shown to play a significant role in gamete interactions.
Erythrocyte glutathione peroxidase (show GPX1 Proteins) activity is modified by single nucleotide polymorphisms in SEPP1 (show SEPP1 Proteins), GPX4 and GPX1 (show GPX1 Proteins) and by estrogens.
neither CYBB (show CYBB Proteins) nor GPX4 are major genetic determinants of diabetic nephropathy, but nevertheless, they could modulate in a gender-specific manner the risk for renal disease in patients with type 1 diabetes.
Phospholipid hydroperoxide glutathione peroxidase (show GPX1 Proteins) is involved in the maintenance of male fertility under cryptorchidism in mice
dramatic motor neuron degeneration and paralysis induced by Gpx4 ablation suggest that ferroptosis inhibition by GPX4 is essential for motor neuron health and survival in vivo
The lack of catalytic activity is the major reason for the embryonic lethality of Gpx4 knockout mice.
Homozygous expression of Gpx4 with a targeted substitution of selenocysteine to serine causes early embryonic death as expected but, unexpectedly, male subfertility in heterozygous mice.
GPx4 suppresses the increase in the VEGF-A (show VEGFA Proteins) protein level, which occurs during the development of pathological CNV, thus partly explaining the protective effect of GPx4 against CNV.
Inducible disruption of Gpx4 causes acute renal failure and early death in an Alox15 (show ALOX15 Proteins)-independent manner
Rat Gpx4 is a moonlighting protein that functions both as a peroxidase, as well as a structural protein.
GPx4-overexpressing mice showed no free fatty acid induced increase in reactive oxygen species and lipid peroxidation
Activity of cutaneous GPx4 is linked to the regulation of COX-2 and hair follicle morphogenesis and provides insight into the function of individual selenoprotein activity in maintaining cutaneous homeostasis.
GPx-4 has an important role in the physiological control of peroxide tone in the bordering cells of the oviductal lumen
Glutathione peroxidase catalyzes the reduction of hydrogen peroxide, organic hydroperoxide, and lipid peroxides by reduced glutathione and functions in the protection of cells against oxidative damage. Human plasma glutathione peroxidase has been shown to be a selenium-containing enzyme and the UGA codon is translated into a selenocysteine. Through alternative splicing and transcription initiation, rat produces proteins that localize to the nucleus, mitochondrion, and cytoplasm. In humans, experimental evidence for alternative splicing exists\; alternative transcription initiation and the cleavage sites of the mitochondrial and nuclear transit peptides need to be experimentally verified.
glutathione peroxidase 4
, phospholipid hydroperoxidase
, phospholipid hydroperoxide glutathione peroxidase, mitochondrial
, sperm nucleus glutathione peroxidase
, phospholipid hydroperoxide glutathione peroxidase, nuclear
, sperm nuclei glutathione peroxidase
, phospholipid hydroperoxide glutathione peroxidase
, glutathione peroxidase 4 (phospholipid hydroperoxidase)