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Merck
CN

G8404

葡萄糖-6-磷酸脱氢酶 来源于肠系膜明串珠菌

recombinant, expressed in E. coli, ammonium sulfate suspension, ≥550 units/mg protein (biuret)

别名:

Entner-Doudoroff酶, G6PD, G6PDH, NADP 葡萄糖 6-磷酸脱氢酶, G-6-P-DH

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关于此项目

化学文摘社编号:
UNSPSC Code:
12352204
NACRES:
NA.54
MDL number:
Specific activity:
≥550 units/mg protein (biuret)
Biological source:
bacterial (Leuconostoc mesenteroides)
Recombinant:
expressed in E. coli
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产品名称

葡萄糖-6-磷酸脱氢酶 来源于肠系膜明串珠菌, recombinant, expressed in E. coli, ammonium sulfate suspension, ≥550 units/mg protein (biuret)

biological source

bacterial (Leuconostoc mesenteroides)

recombinant

expressed in E. coli

form

ammonium sulfate suspension

specific activity

≥550 units/mg protein (biuret)

mol wt

128 kDa

storage condition

(Tightly closed)

technique(s)

cell culture | mammalian: suitable

UniProt accession no.

foreign activity

creatine phosphokinase, glutathione reductase, myokinase, NADH oxidase, NADPH oxidase, phosphoglucomutase, 6-phosphogluconic dehydrogenase, phosphoglucose isomerase, lactic dehydrogenase, hexokinase ≤0.01%

storage temp.

2-8°C

Quality Level

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Application

葡萄糖-6-磷酸脱氢酶已用于:

  • 测试玉米胚乳发育过程中的酮糖还原酶活性。
  • 测定冠心病患者血清中甘露糖的水平
  • 研究其对细胞外聚合物 (EPS) 提取物的反应活性,超声法测定细胞裂解液
  • 测定培养人体肌肉卫星细胞的葡萄糖摄入情况

Biochem/physiol Actions

G6PD可为所有细胞提供还原动力(如烟酰胺腺嘌呤二核苷酸磷酸 (NADPH)),使细胞能够平衡氧化压力。G6PD基因突变与 X 连锁G6PD缺陷有关——这是一种遗传性基因缺陷,包括新生儿黄疸和急性溶血性贫血等。
葡萄糖-6-磷酸脱氢酶(G6PD)催化葡萄糖-6-磷酸转化为6-磷酸葡糖酸内酯,作为磷酸戊糖途径的第一步。

General description

葡萄糖6-磷酸脱氢酶(G-6-P-DH)是磷酸戊糖途径第一步的关键调节酶。G-6-P-DH是一种糖蛋白,分子量为 128 kDa(凝胶过滤)。G6PD 是二聚体,每个亚基上有一个活性位点。

研究领域:细胞信号传导

Other Notes

在 NAD 存在下,在pH 7.8,30°C 下,1 个单位将每分钟氧化 1.0 μmol D-6-磷酸葡萄糖至 6-磷酸-D-葡萄糖酸盐。
每批产品的体积都不一样,可用下列数据计算:
例如,批号0000114274产品
846单位/每mg蛋白
9 mg蛋白/mL
7614单位/mL
得出,G8404-1000U ≈ 132 ul

Physical form

用 3.2 M (NH 4 ) 2 SO 4 (含 50 mM Tris 和 1 mM MgCl 2 ,pH 7.5)混悬

存储类别

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

常规特殊物品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Hemang M Parikh et al.
BMC endocrine disorders, 21(1), 32-32 (2021-03-01)
Insulin resistance (IR) in skeletal muscle is a key feature of the pre-diabetic state, hypertension, dyslipidemia, cardiovascular diseases and also predicts type 2 diabetes. However, the underlying molecular mechanisms are still poorly understood. To explore these mechanisms, we related global
Angelo Minucci et al.
IUBMB life, 61(1), 27-34 (2008-10-23)
Glucose 6-phosphate dehydrogenase (G6PD) deficiency is the most common defect of red blood cells. Although some different laboratory techniques or methods are employed for the biochemical screening, a strict relationship between biochemists, clinicians, and molecular biologists is necessary for a
Charles-David Dubé et al.
AMB Express, 9(1), 23-23 (2019-02-08)
Extracellular polymeric substances (EPS) play major roles in the efficacy of biofilms such as anaerobic granules, ranging from structural stability to more specific functions. The EPS of three granular anaerobic sludges of different origins were studied and compared. Particularly, the
M D Cappellini et al.
Lancet (London, England), 371(9606), 64-74 (2008-01-08)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzyme defect, being present in more than 400 million people worldwide. The global distribution of this disorder is remarkably similar to that of malaria, lending support to the so-called malaria protection
Cara A Griffiths et al.
Nature, 540(7634), 574-578 (2016-12-16)
The pressing global issue of food insecurity due to population growth, diminishing land and variable climate can only be addressed in agriculture by improving both maximum crop yield potential and resilience. Genetic modification is one potential solution, but has yet

商品

Instructions for working with enzymes supplied as ammonium sulfate suspensions

以硫酸铵悬浮液形式提供的酶的使用指南

实验方案

To measure glucose-6-phosphate dehydrogenase activity, beta-nicotinamide adenine dinucleotide phosphate is used in a spectrophotometric rate determination assay at 340 nm.

在测定6-磷酸葡萄糖脱氢酶活性时,使用β-烟酰胺腺嘌呤二核苷酸磷酸在340 nm处通过分光光度法进行测定。

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