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Merck
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主要文件

SRP8010

Sigma-Aldrich

GPX1 human

recombinant, expressed in E. coli, His tagged, >90% (SDS-PAGE)

别名:

细胞谷胱甘肽过氧化物酶

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About This Item

分類程式碼代碼:
12352200
NACRES:
NA.32

生物源

human

重組細胞

expressed in E. coli

籤條

His tagged

化驗

>90% (SDS-PAGE)

形狀

lyophilized

分子量

~25 kDa by SDS-PAGE

包裝

pkg of 10 μg

儲存條件

avoid repeated freeze/thaw cycles

雜質

<1 EU/μg endotoxin, tested

顏色

white

UniProt登錄號

運輸包裝

wet ice

儲存溫度

−20°C

基因資訊

human ... GPX1(2876)

一般說明

GPX1 (glutathione peroxidase 1) is a selenoprotein and the gene is mapped to human chromosome 3p21.3. It is present in the cytoplasm and is widely expressed.

生化/生理作用

GPX1 (glutathione peroxidase 1) is responsible for scavenging free radicals and derivatives. GPXs reduces lipid hydroperoxides to the corresponding alcohols as well as free hydrogen peroxide to water. Mutations in the GPX1 gene are associated with nonalcoholic fatty liver disease (NAFLD) susceptibility. Mutation in GPX1 at C594T is linked with oxidative stress-associated disorders, including prostate cancer and bladder cancer.

外觀

Lyophilized from 55 mM TRIS-HCl, pH 8.2, containing 150 mM NaCl, 1 mM DTT.

重構

Reconstitute with 100 μL deionized water.

其他說明

Human GPX1 (aa 1-201) is fused at the C-terminus to a His-tag.

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Glutathione Peroxidase Level in Patients with Vitiligo: A Meta-Analysis.
Xiao BH, et al.
BioMed Research International, 2016, 3029810-3029810 (2016)
Association of polymorphisms of adiponectin gene promoter-11377C/G, glutathione peroxidase-1 gene C594T, and cigarette smoking in nonalcoholic fatty liver disease.
Zhang CX, et al.
Journal of the Chinese Medical Association : JCMA, 79, 195-195 (2016)
Influence of Gender and SNPs in GPX1 Gene on Biomarkers of Selenium Status in Healthy Brazilians.
Donadio JL, et al.
Nutrients, 8, E81-E81 (2016)
Manon Ros et al.
Nature cell biology, 22(11), 1371-1381 (2020-10-21)
Tumour growth and invasiveness require extracellular matrix (ECM) degradation and are stimulated by the GALA pathway, which induces protein O-glycosylation in the endoplasmic reticulum (ER). ECM degradation requires metalloproteases, but whether other enzymes are required is unclear. Here, we show

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