G6880
α-甘油磷酸脱氢酶 来源于兔肌肉
Type X, lyophilized powder, ≥100 units/mg protein
别名:
sn-甘油-3-磷酸:NAD+ 2-氧化还原酶, sn-甘油-3-磷酸脱氢酶 来源于兔肌肉
应用
α-甘油磷酸脱氢酶可用于2-脱氧核糖-5-磷酸醛缩酶（DERA）裂解（反醛醇）检测。
生化/生理作用
α-甘油磷酸脱氢酶可催化二羟基丙酮转化为甘油磷酸酯。
外形
冻干粉，无硫酸盐，含缓冲柠檬酸盐和 EDTA
分析说明
由缩二脲确定的蛋白质
其他说明
一个酶活性单位是指在pH 7.4、25℃下，每分钟将1.0 μM二羟丙酮磷酸盐转化为α-甘油磷酸酯所需的酶量。
警示用语：
Danger
危险声明
预防措施声明
危险分类
Resp. Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
低风险生物材料
此项目有
Grace DeSantis et al.
Bioorganic & medicinal chemistry, 11(1), 43-52 (2002-12-07)
2-Deoxyribose-5-phosphate aldolase (DERA, EC 4.1.2.4) catalyzes the reversible aldol reaction between acetaldehyde and D-glyceraldehyde-3-phosphate to generate D-2-deoxyribose-5-phosphate. It is unique among the aldolases as it catalyzes the reversible asymmetric aldol addition reaction of two aldehydes. In order to expand the
Yongxiu Fan et al.
Parasitology research, 109(3), 621-626 (2011-03-17)
Glycerol 3-phosphate dehydrogenase (GPD) plays an important role in the energy metabolism and nutrition metabolism. In order to know about the biological functions of GPD of Clonorchis sinensis (C. sinensis), we identified a complete gene coding GPD from C. sinensis
Feng Peng et al.
Yeast (Chichester, England), 27(2), 115-121 (2009-12-17)
In this study, a novel glycerol-3-phosphate dehydrogenase (NAD(+)) (EC1.1.1.8) gene (PfGPD) was cloned from halotolerant yeast Pichia farinosa, using degenerate reverse transcription (RT)-PCR and rapid amplification of cDNA ends (RACE) methods. The full-length cDNA of the PfGPD gene is 1403
Kui-Yi Xing et al.
Investigative ophthalmology & visual science, 51(12), 6598-6604 (2010-07-09)
To investigate the effect of age on the key oxidation repair enzymes of the thioltransferase (TTase) and thioredoxin (TRx) systems in the human lens. Twenty-three normal human lenses (donor ages, 19-77 years) were grouped into second, third, fifth, sixth, and
Zhong-peng Guo et al.
Journal of industrial microbiology & biotechnology, 38(8), 935-943 (2010-09-09)
The GPD2 gene, encoding NAD(+)-dependent glycerol-3-phosphate dehydrogenase in an industrial ethanol-producing strain of Saccharomyces cerevisiae, was deleted. And then, either the non-phosphorylating NADP(+)-dependent glyceraldehyde-3-phosphate dehydrogenase (GAPN) from Bacillus cereus, or the NADP(+)-dependent glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from Kluyveromyces lactis, was expressed
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