Recombinant Human CNDP1 Protein (His Tag) (PKSH033451)

For research use only.
Synonyms | Beta-Ala-His Dipeptidase, CN1, CNDP Dipeptidase 1, CNDP1, CPGL2, Carnosine Dipeptidase 1, Glutamate Carboxypeptidase-Like Protein 2, HsT2308, Serum Carnosinase |
Species | Human |
Expression Host | HEK293 Cells |
Sequence | Pro28-His507 |
Accession | AAI13513.1 |
Calculated Molecular Weight | 54.9 kDa |
Observed Molecular Weight | 60-90 kDa |
Tag | C-His |
Bio-activity | Not validated for activity |
Purity | > 95 % as determined by reducing SDS-PAGE. |
Endotoxin | < 1.0 EU per μg of the protein as determined by the LAL method. |
Storage | Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles. |
Shipping | This product is provided as liquid. It is shipped at frozen temperature with blue ice/gel packs. Upon receipt, store it immediately at < - 20°C. |
Formulation | Supplied as a 0.2 μm filtered solution of 20mM Tris-HCl, 150mM NaCl, pH 7.5. |
Reconstitution | Not Applicable |
Background | Carnosine Dipeptidase 1 (CNDP1) belongs to the M20 metalloprotease family. CNDP1 is specifically expressed in the brain; serum and adult nervous central system. It is identified as human carnosinase. CNDP1 contains trinucleotide (CTG) repeat length polymorphism in the coding region and is inhibited by the metal chelator 1;10-o-phenantrolin. In addition; CNDP1 can hydrolyse the beta-Ala|-His dipeptide (carnosine); anserine; Xaa-|-His dipeptides and other dipeptides including homocarnosine. CNDP1 deficiency has been associated with homocarnosinosis disease. |
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