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PEPD Protein, Human, Recombinant

(Synonyms: Xaa-Pro dipeptidase, Prolinedipeptidase, PRD, PeptidaseD, PEPD, Imidodipeptidase) Copy Product Info

Synonyms: Xaa-Pro dipeptidase, Prolinedipeptidase, PRD, PeptidaseD, PEPD, Imidodipeptidase

Catalog No. TMPJ-00540 Copy Product Info
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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Pack SizePriceUSA StockGlobal StockQuantity
10 µg$1837-10 days7-10 days
20 µg$2927-10 days7-10 days
50 µg$5457-10 days7-10 days
100 µg$8137-10 days7-10 days
200 µg$1,1907-10 days7-10 days
500 µg$2,0707-10 days7-10 days
1 mg$2,9707-10 days7-10 days
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Batch Information

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Purity:Greater than 90% as determined by reducing SDS-PAGE. (QC verified)
Appearance:Liquid
Color:Transparent
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Product Introduction

Bioactivity
Bioactivity
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.
Description
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.
Species
Human
Expression System
E. coli
TagTag Free
Accession NumberAAH28295.1
Amino AcidAla2-Lys493
ConstructionAla2-Lys493
Protein Purity
Greater than 90% as determined by reducing SDS-PAGE. (QC verified)
Endotoxin< 0.1 ng/µg (1 EU/µg) as determined by LAL test.
FormulationSupplied as a 0.2 μm filtered solution of 25 mM Tris-HCl, 100 mM Glycine, 10% Glycerol, pH 8.5.
SynonymsXaa-Pro dipeptidase, Prolinedipeptidase, PRD, PeptidaseD, PEPD, Imidodipeptidase
Research Background
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.
Chemical Properties
Molecular Weight60 KDa (reducing condition)
Storage & Solubility Information
ShippingProteins are shipped with blue ice.
StorageLyophilized 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.

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Related Tags: PEPD Protein, Human, Recombinant chemical structure | PEPD Protein, Human, Recombinant molecular weight