The GPX4 Rabbit Monoclonal Antibody is a valuable tool for researchers studying GPX4, a key enzyme involved in protecting cells from oxidative damage and ferroptosis. This antibody, produced in rabbits, exhibits high reactivity with human samples and has been validated for use in Western blot applications. By binding specifically to the GPX4 protein, this antibody enables accurate detection and analysis in a variety of cell types, making it ideal for investigations in the fields of oxidative stress, cell death, and cancer biology.GPX4 is a crucial antioxidant enzyme that plays a critical role in protecting cells from oxidative stress and lipid peroxidation. Dysregulation of GPX4 has been implicated in various diseases, including cancer, neurodegenerative disorders, and cardiovascular conditions.
Through further research on GPX4 activity and regulation, scientists hope to uncover new therapeutic targets for treating diseases associated with oxidative damage and cell death.Overall, the GPX4 Rabbit Monoclonal Antibody is a valuable asset for researchers seeking to deepen their understanding of GPX4 function and explore its potential implications in health and disease. Its high specificity and reactivity make it a reliable tool for conducting Western blot analyses and advancing research in the fields of oxidative biology and cancer therapeutics.
Product Name:
GPX4 Rabbit Monoclonal Antibody
SKU:
CAB11243
Size:
20uL, 100uL
Isotype:
IgG
Host Species:
Rabbit
Reactivity:
Human,Mouse,Rat
Immunogen:
A synthetic peptide corresponding to a sequence within amino acids 1-100 of human GPX4 (P36969).
The protein encoded by this gene belongs to the glutathione peroxidase family, members of which catalyze the reduction of hydrogen peroxide, organic hydroperoxides and lipid hydroperoxides, and thereby protect cells against oxidative damage. Several isozymes of this gene family exist in vertebrates, which vary in cellular location and substrate specificity. This isozyme has a high preference for lipid hydroperoxides and protects cells against membrane lipid peroxidation and cell death. It is also required for normal sperm development; thus, it has been identified as a 'moonlighting' protein because of its ability to serve dual functions as a peroxidase, as well as a structural protein in mature spermatozoa. Mutations in this gene are associated with Sedaghatian type of spondylometaphyseal dysplasia (SMDS). This isozyme is also a selenoprotein, containing the rare amino acid selenocysteine (Sec) at its active site. Sec is encoded by the UGA codon, which normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, designated the Sec insertion sequence (SECIS) element, that is necessary for the recognition of UGA as a Sec codon, rather than as a stop signal. Transcript variants resulting from alternative splicing or use of alternate promoters have been described to encode isoforms with different subcellular localization.
Purification Method:
Affinity purification
Gene ID:
2879
Clone Number:
ARC0558
Storage Buffer:
Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,0.05% BSA,50% glycerol,pH7.3.
Western blot analysis of various lysates using GPX4 Rabbit mAb (CAB11243) at 1：1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution.Lysates/proteins: 25μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit (AbGn00020).Exposure time: 10s.
