PEPD Protéine

N° du produit ABIN7318881

Détail du produit

Antigène: PEPD (Peptidase D (PEPD))

Type de proteíne: Recombinant

Origine: Humain

Source: Escherichia coli (E. coli)

Fonction: Recombinant Human Peptidase D/PEPD Protein

Séquence: Ala2-Lys493

Attributs du produit: Recombinant Human Peptidase D is produced by our E.coli expression system and the target gene encoding Ala2-Lys493 is expressed.

Pureté: > 95 % as determined by reducing SDS-PAGE.

niveau d'endotoxine: < 1.0 EU per μg as determined by the LAL method.

Information d'application

Restrictions: For Research Use only

Stockage

Format: Frozen, Liquid

Buffer: Supplied as a 0.2 μm filtered solution of 20 mM PB,150 mM NaCl, pH 7.4.

Stock: -20 °C

Stockage commentaire: Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.

Détail du antigène

Antigène: PEPD (Peptidase D (PEPD))

Autre désignation: Peptidase D/PEPD (PEPD Produits)

Synonymes: MGC89151 Protein, DDBDRAFT_0190220 Protein, DDBDRAFT_0266378 Protein, DDB_0190220 Protein, DDB_0266378 Protein, PROLIDASE Protein, cb1000 Protein, fj78g11 Protein, wu:fj78g11 Protein, prolidase Protein, Pep-4 Protein, Pep4 Protein, peptidase D Protein, peptidase D L homeolog Protein, pepd Protein, pepD Protein, PEPD Protein, pepd.L Protein, Pepd Protein

Sujet:

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.

Synonym: Xaa-Pro dipeptidase, Imidodipeptidase, PeptidaseD, Prolinedipeptidase, PRD, PEPD.

Poids moléculaire: 54.5 kDa

UniProt: P12955