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PEPD Protein, Human, Recombinant

PEPD Protein, Human, Recombinant

产品编号 TMPJ-00540
别名: PRD, Imidodipeptidase, PEPD, PeptidaseD, Prolinedipeptidase, Xaa-Pro dipeptidase

PEPD belongs to the peptidase M24B family of Eukaryotic-type prolidase subfamily. PEPD is a cytosolic dipeptidase that hydrolyzes dipeptides with proline or hydroxyproline at the carboxy terminus. It is important in collagen metabolism because of the high levels of imino acids. Defects in PEPD are a cause of prolidase deficiency which is an autosomal recessive disorder associated with iminodipeptiduria.

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PEPD Protein, Human, Recombinant
规格 价格/CNY 货期 数量
10 μg ¥ 1,170 5日内发货
50 μg ¥ 3,470 5日内发货
500 μg ¥ 13,200 5日内发货
1 mg ¥ 18,900 5日内发货
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产品目录号及名称: PEPD Protein, Human, Recombinant (TMPJ-00540)
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产品性质
产品描述 PEPD belongs to the peptidase M24B family of Eukaryotic-type prolidase subfamily. PEPD is a cytosolic dipeptidase that hydrolyzes dipeptides with proline or hydroxyproline at the carboxy terminus. It is important in collagen metabolism because of the high levels of imino acids. Defects in PEPD are a cause of prolidase deficiency which is an autosomal recessive disorder associated with iminodipeptiduria.
种属 Human
表达系统 E. coli
标签 Tag Free
蛋白编号 AAH28295.1
别名 PRD, Imidodipeptidase, PEPD, PeptidaseD, Prolinedipeptidase, Xaa-Pro dipeptidase
氨基酸序列 Ala2-Lys493
蛋白构建 Ala2-Lys493
蛋白纯度 Greater than 90% as determined by reducing SDS-PAGE. (QC verified)
分子量 60 KDa (reducing condition)
内毒素 < 0.1 ng/µg (1 EU/µg) as determined by LAL test.
缓冲液 Supplied as a 0.2 μm filtered solution of 25 mM Tris-HCl, 100 mM Glycine, 10% Glycerol, pH 8.5.
存储

Lyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at-80℃. For reconstituted proteinsolutions, the solution can be stored at -20°c to -80'c for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.

运输方式

In general, Lyophilized powders are shipping with blue ice. Solutions are shipping with dry ice.

研究背景 PEPD belongs to the peptidase M24B family of Eukaryotic-type prolidase subfamily. PEPD is a cytosolic dipeptidase that hydrolyzes dipeptides with proline or hydroxyproline at the carboxy terminus. It is important in collagen metabolism because of the high levels of imino acids. Defects in PEPD are a cause of prolidase deficiency which is an autosomal recessive disorder associated with iminodipeptiduria.

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Keywords

PEPD Protein, Human, Recombinant PRD Imidodipeptidase PEPD PeptidaseD Prolinedipeptidase Xaa-Pro dipeptidase recombinant recombinant-proteins proteins protein

 

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