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Conditions of optimal BDH1 Enzyme 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
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Introduction
D-Beta-Hydroxybutyrate Dehydrogenase Mitochondrial (BDH) is a member of the short-chain dehydrogenases/reductases (SDR) family. BDH is localized in the mitochondrion matrix. BDH forms a homotetrameric lipid-requiring enzyme of the mitochondrial membrane and has a specific necessity for phosphatidylcholine for optimal enzymatic activity. BDH catalyzes the interconversion of acetoacetate and (R)-3-hydroxybutyrate, the 2 main ketone bodies formed during fatty acid catabolism.
BP001791-ENZ-215: Recombinant Human D-Beta-Hydroxybutyrate Dehydrogenase Mitochondrial (BDH1) Enzyme
Source: E. coli-derived.
A single, non-glycosylated polypeptide chain containing 318 amino acids (47-343) and having a molecular mass of 35.3 kDa. BDH1 is fused to a 21 amino acid His-tag at N-terminus.
Purity: > 85% by SDS-PAGE.
Formulation: The BDH1 solution (0.25 mg/ml) contains 20 mM Tris-HCl buffer (pH8.0), 30% glycerol, 0.2 M NaCl, 2 mM DTT and 0.1 mM PMSF.
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.
Other BDH1 Enzymes:
Recombinant Human BDH1 Enzyme
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