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PEPD Protein, Human, Recombinant

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货号 TMPJ-00540

别名 Xaa-Pro dipeptidase, Prolinedipeptidase, PRD, PeptidaseD, PEPD, Imidodipeptidase

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.

PEPD Protein, Human, Recombinant
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PEPD Protein, Human, Recombinant

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货号 TMPJ-00540 别名 Xaa-Pro dipeptidase, Prolinedipeptidase, PRD, PeptidaseD, PEPD, Imidodipeptidase

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.

规格价格库存数量
5 μg
¥ 693
6-8日内发货
10 μg
¥ 1,170
6-8日内发货
20 μg
¥ 1,860
5日内发货
50 μg
¥ 3,470
5日内发货
100 μg
¥ 5,180
5日内发货
200 μg
¥ 7,730
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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选择批次:
纯度: Greater than 90% as determined by reducing SDS-PAGE. (QC verified)
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产品介绍


生物活性
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.
生物活性
Activity has not been tested. It is theoretically active, but we cannot guarantee it. If you require protein activity, we recommend choosing the eukaryotic expression version first.
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.
种属
Human
表达系统
E. coli
标签Tag Free
蛋白编号AAH28295.1
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)
缓冲液Supplied as a 0.2 μm filtered solution of 25 mM Tris-HCl, 100 mM Glycine, 10% Glycerol, pH 8.5.
别名Xaa-Pro dipeptidase, Prolinedipeptidase, PRD, PeptidaseD, PEPD, Imidodipeptidase
内毒素< 0.1 ng/µg (1 EU/µg) as determined by LAL test.
化学信息
分子量60 KDa (reducing condition)
储存&溶解度
运输方式In general, Lyophilized powders are shipping with blue ice. Solutions are shipping with dry ice.
存储Lyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, 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.

计算器

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  • 重组蛋白稀释 计算器
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技术支持

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