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PHGDH Protein, Human, Recombinant (His)

カタログ番号 TMPY-02801
別名: 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)
パッケージサイズ 在庫状況 単価(税別)
100 μg 在庫あり ¥ 98,500
200 μg 約5 days ¥ 168,000
500 μg 約5 days ¥ 340,000
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生物学的特性に関する説明
Technical Params
Product Properties
参考文献
生物学的情報 Testing in progress
説明 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.
Species Human
Expression Host E. coli
Tag His
Accession Number O43175
別名 phosphoglycerate dehydrogenase, HEL-S-113, 3PGDH, NLS1, PHGDHD, PGDH, NLS, SERA, PGAD, 3-PGDH, PGD, PDG
Construction 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.
Protein Purity > 90 % as determined by SDS-PAGE

分子量 58kDa (predicted)
Endotoxin Please contact us for more information.
Formulation 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.
Reconstitution A hardcopy of datasheet with reconstitution instructions is sent along with the products. Please refer to it for detailed information.
Stability & Storage

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.

Shipping

Solution. It is shipped out with blue ice.

Research Background 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.

参考文献

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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