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| Catalog No. | Product Name | Size | List Price (US$) | Quantity |
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Conditions of optimal MPI Enyzme performance should be determined experimentally by the investigator.
Price/availability/specifications subject to change without notice. Unless otherwise indicated, our catalog and customized products are for research use only and not intended for human or animal diagnostic or therapeutic use.
Phone: 1-617-401-8149
Fax: 1-617-606-5019
Email: message@sydlabs.com
Or leave a message with a formal purchase
order (PO) Or credit card.
Introduction
MPI is a member of the mannose-6-phosphate isomerase type 1 family. Although MPI is expressed in all tissues, it can be found more abundantly in heart, brain and skeletal muscle. Localized to the cytoplasm, MPI exploits zinc as a cofactor and catalyzes the interconversion of fructose-6-phosphate and mannose-6-phosphate. Mutations in the MPI gene are the cause of carbohydrate-deficient glycoprotein syndrome, type Ib.
BP002551-ENZ-169: Recombinant Human Mannose Phosphate Isomerase (MPI) Enzyme
Source: E. coli-derived.
A single, non-glycosylated polypeptide chain containing 382 amino acids (1-362) and having a molecular mass of 41.9 kDa. The MPI is fused to a 20 amino acid His-Tag at N-terminus.
Purity: > 90% as determined by SDS-PAGE.
Formulation: The MPI solution (0.5 mg/ml) contains 20 mM Tris-HCl buffer (pH 8.0), 0.4 M Urea and 5% glycerol.
Shipping: The product is shipped with ice pack. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
12 months from date of receipt, -20 to -70°C as supplied.
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