Human Recombinant GPX4 protein, His Tag (V2LY-0526-LY4402)

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Basic Information

Expressed Host
E. coli
Protein Species
Human
Tag
His Tag
Protein Construction
This product is Human Recombinant GPX4 protein, His Tag consist of Amino Acid: 26-197 and predicts a molecular mass of 20.59 kDa.
Molecule Mass
20.59 kDa
Sequence
Amino Acid: 26-197
Species
Human

Formulations & Storage [For reference only, actual COA shall prevail!]

Purity
≥95% as determined by SDS-PAGE.
Endotoxin
Please contact us for more information.
Format
Lyophilized
Reconstitution
Allow the vial and reconstitution buffer to equilibrate to room temperature. Briefly centrifuge or tap down the vial to ensure that all lyophilized powder is collected at the bottom of the vial. For the reconstitution of this product, we recommend adding PBS or sterile water to achieve a final antibody concentration of 1 mg/mL. Allow the vial to reconstitute for 10-15 minutes at room temperature with gentle agitation. Avoid vigorous shaking that can cause foaming and antibody denaturation. Aliquot into volumes based on your experiment and store liquid protein at -20°C or -80°C for long time.
Buffer
Lyophilized from sterile PBS
Preservative
None
Storage
Samples are stable for up to twelve months from date of receipt at -20°C to -80°C. Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
More Infomation

Target

Full Name
Glutathione Peroxidase 4
Function
Essential antioxidant peroxidase that directly reduces phospholipid hydroperoxide even if they are incorporated in membranes and lipoproteins (By similarity).

Can also reduce fatty acid hydroperoxide, cholesterol hydroperoxide and thymine hydroperoxide (By similarity).

Plays a key role in protecting cells from oxidative damage by preventing membrane lipid peroxidation (By similarity).

Required to prevent cells from ferroptosis, a non-apoptotic cell death resulting from an iron-dependent accumulation of lipid reactive oxygen species (PubMed:24439385).

The presence of selenocysteine (Sec) versus Cys at the active site is essential for life: it provides resistance to overoxidation and prevents cells against ferroptosis (By similarity).

The presence of Sec at the active site is also essential for the survival of a specific type of parvalbumin-positive interneurons, thereby preventing against fatal epileptic seizures (By similarity).

May be required to protect cells from the toxicity of ingested lipid hydroperoxides (By similarity).

Required for normal sperm development and male fertility (By similarity).

Essential for maturation and survival of photoreceptor cells (By similarity).

Plays a role in a primary T-cell response to viral and parasitic infection by protecting T-cells from ferroptosis and by supporting T-cell expansion (By similarity).

Plays a role of glutathione peroxidase in platelets in the arachidonic acid metabolism (PubMed:11115402).

Reduces hydroperoxy ester lipids formed by a 15-lipoxygenase that may play a role as down-regulator of the cellular 15-lipoxygenase pathway (By similarity).
Biological Process
Aging Source: Ensembl
Arachidonic acid metabolic process Source: UniProtKB
Chromatin organization Source: Ensembl
Glutathione metabolic process Source: Ensembl
Lipoxygenase pathway Source: UniProtKB
Long-chain fatty acid biosynthetic process Source: Reactome
Negative regulation of ferroptosis Source: UniProtKB
Phospholipid metabolic process Source: UniProtKB
Protein polymerization Source: CAFA
Regulation of inflammatory response Source: Ensembl
Response to estradiol Source: Ensembl
Response to oxidative stress Source: UniProtKB
Spermatogenesis Source: UniProtKB
Cellular Location
Isoform Mitochondrial: Mitochondrion
Isoform Cytoplasmic: Cytoplasm
Involvement in disease
Spondylometaphyseal dysplasia, Sedaghatian type (SMDS):
A form of spondylometaphyseal dysplasia, a group of short stature disorders distinguished by abnormalities in the vertebrae and the metaphyses of the tubular bones. SMDS is a neonatal lethal form characterized by severe metaphyseal chondrodysplasia with mild limb shortening, platyspondyly, cardiac conduction defects, and central nervous system abnormalities.

Weaver, K., & Skouta, R. (2022). The selenoprotein glutathione peroxidase 4: from molecular mechanisms to novel therapeutic opportunities. Biomedicines, 10(4), 891.

Ursini, F., Travain, V. B., Cozza, G., Miotto, G., Roveri, A., Toppo, S., & Maiorino, M. (2022). A white paper on Phospholipid Hydroperoxide Glutathione Peroxidase (GPx4) forty years later. Free Radical Biology and Medicine, 188, 117-133.

Huang, J., Chen, G., Wang, J., Liu, S., & Su, J. (2022). Platycodin D regulates high glucose-induced ferroptosis of HK-2 cells through glutathione peroxidase 4 (GPX4). Bioengineered, 13(3), 6627-6637.

Xu, S., Wu, B., Zhong, B., Lin, L., Ding, Y., Jin, X., ... & Xu, D. (2021). Naringenin alleviates myocardial ischemia/reperfusion injury by regulating the nuclear factor-erythroid factor 2-related factor 2 (Nrf2)/System xc-/glutathione peroxidase 4 (GPX4) axis to inhibit ferroptosis. Bioengineered, 12(2), 10924-10934.

Zhang, X., Sui, S., Wang, L., Li, H., Zhang, L., Xu, S., & Zheng, X. (2020). Inhibition of tumor propellant glutathione peroxidase 4 induces ferroptosis in cancer cells and enhances anticancer effect of cisplatin. Journal of cellular physiology, 235(4), 3425-3437.

Wei, Y., Lv, H., Shaikh, A. B., Han, W., Hou, H., Zhang, Z., ... & Shang, P. (2020). Directly targeting glutathione peroxidase 4 may be more effective than disrupting glutathione on ferroptosis-based cancer therapy. Biochimica et Biophysica Acta (BBA)-General Subjects, 1864(4), 129539.

Zhang, Z., Wu, Y. U., Yuan, S., Zhang, P., Zhang, J., Li, H., ... & Chen, G. (2018). Glutathione peroxidase 4 participates in secondary brain injury through mediating ferroptosis in a rat model of intracerebral hemorrhage. Brain research, 1701, 112-125.

Kinowaki, Y., Kurata, M., Ishibashi, S., Ikeda, M., Tatsuzawa, A., Yamamoto, M., ... & Yamamoto, K. (2018). Glutathione peroxidase 4 overexpression inhibits ROS-induced cell death in diffuse large B-cell lymphoma. Laboratory Investigation, 98(5), 609-619.

Li, C., Deng, X., Xie, X., Liu, Y., Friedmann Angeli, J. P., & Lai, L. (2018). Activation of glutathione peroxidase 4 as a novel anti-inflammatory strategy. Frontiers in Pharmacology, 9, 1120.

Li, C., Deng, X., Zhang, W., Xie, X., Conrad, M., Liu, Y., ... & Lai, L. (2018). Novel allosteric activators for ferroptosis regulator glutathione peroxidase 4. Journal of medicinal chemistry, 62(1), 266-275.

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For research use only. Not intended for any clinical use.

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