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PHGDH Protein, Human, Recombinant (His)

PHGDH Protein, Human, Recombinant (His)

产品编号 TMPY-02801
别名: phosphoglycerate dehydrogenase, HEL-S-113, 3PGDH, NLS1, PHGDHD, PGDH, NLS, SERA, PGAD, 3-PGDH, PGD, PDG

PHGDH is a member of the D-isomer specific 2-hydroxyacid dehydrogenase family. This new family consists of D-isomer-stereospecific enzymes. The conserved residues in this family appear to be the residues involved in the substrate binding and the catalytic reaction, and thus to be targets for site-directed mutagenesis. A number of NAD-dependent 2-hydroxyacid dehydrogenases which seem to be specific for the D-isomer of their substrate have been shown to be functionally and structurally related. PHGDH catalyzes the transition of 3-phosphoglycerate into 3-phosphohydroxypyruvate, which is the first and rate-limiting step in the phosphorylated pathway of serine biosynthesis, using NAD+/NADH as a cofactor. Overexpression of PHGDH may cause certain breast cancers. Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency which is characterized by congenital microcephaly, psychomotor retardation, and seizures.

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PHGDH Protein, Human, Recombinant (His)
规格 价格/CNY 货期 数量
100 μg ¥ 4,240 现货
200 μg ¥ 7,240 5日内发货
500 μg ¥ 14,660 5日内发货
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产品目录号及名称: PHGDH Protein, Human, Recombinant (His) (TMPY-02801)
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生物活性 Testing in progress
产品描述 PHGDH is a member of the D-isomer specific 2-hydroxyacid dehydrogenase family. This new family consists of D-isomer-stereospecific enzymes. The conserved residues in this family appear to be the residues involved in the substrate binding and the catalytic reaction, and thus to be targets for site-directed mutagenesis. A number of NAD-dependent 2-hydroxyacid dehydrogenases which seem to be specific for the D-isomer of their substrate have been shown to be functionally and structurally related. PHGDH catalyzes the transition of 3-phosphoglycerate into 3-phosphohydroxypyruvate, which is the first and rate-limiting step in the phosphorylated pathway of serine biosynthesis, using NAD+/NADH as a cofactor. Overexpression of PHGDH may cause certain breast cancers. Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency which is characterized by congenital microcephaly, psychomotor retardation, and seizures.
种属 Human
表达系统 E. coli
标签 His
蛋白编号 O43175
别名 phosphoglycerate dehydrogenase, HEL-S-113, 3PGDH, NLS1, PHGDHD, PGDH, NLS, SERA, PGAD, 3-PGDH, PGD, PDG
蛋白构建 A DNA sequence encoding the mature form of human PHGDH (O43175) (Met 1-Phe 533) was fused with a polyhistidine tag at the C-terminus and an initial Met at the N-terminus.
蛋白纯度 > 90 % as determined by SDS-PAGE

TargetMol

分子量 58kDa (predicted)
内毒素 Please contact us for more information.
缓冲液 Supplied as sterile PBS, 100mM Arg, 0. 1% Tween20, 20% glycerol, pH 8.0. Pleasecon tact usfor any concerns or special requirements. Please refer to the specific buffer information in the hard copy of CoA.
复溶方法 A hardcopy of datasheet with reconstitution instructions is sent along with the products. Please refer to it for detailed information.
存储

Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.

运输方式

Solution. It is shipped out with blue ice.

研究背景 PHGDH is a member of the D-isomer specific 2-hydroxyacid dehydrogenase family. This new family consists of D-isomer-stereospecific enzymes. The conserved residues in this family appear to be the residues involved in the substrate binding and the catalytic reaction, and thus to be targets for site-directed mutagenesis. A number of NAD-dependent 2-hydroxyacid dehydrogenases which seem to be specific for the D-isomer of their substrate have been shown to be functionally and structurally related. PHGDH catalyzes the transition of 3-phosphoglycerate into 3-phosphohydroxypyruvate, which is the first and rate-limiting step in the phosphorylated pathway of serine biosynthesis, using NAD+/NADH as a cofactor. Overexpression of PHGDH may cause certain breast cancers. Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency which is characterized by congenital microcephaly, psychomotor retardation, and seizures.

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Keywords

PHGDH Protein, Human, Recombinant (His) NLS-1 phosphoglycerate dehydrogenase HEL-S-113 3PGDH NLS1 PHGDHD HEL-S 113 HEL-S113 PGDH NLS SERA PGAD NLS 1 3-PGDH PGD PDG recombinant recombinant-proteins proteins protein

 

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