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Conditions of optimal LCAD 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.
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Introduction:
Long-chain specific acyl-CoA dehydrogenase, mitochondrial (ACADL), is a member of the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. ACADL is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in ACADL are the cause of acyl-CoA dehydrogenase very long-chain deficiency, leading to nonketotic hypoglycemia.
BP001342-ENZ-190: Recombinant Human Long-chain specific acyl-CoA dehydrogenase mitochondrial
Source: E. coli-derived.
A single, non-glycosylated polypeptide chain containing 421 amino acids (31-430) and having a molecular mass of 46.7 kDa. ACADL is fused to a 21 amino acid His-tag at N-terminus.
Purity > 85%, by SDS-PAGE.
Formulation: The ACADL solution (1 ug/ml) contains 20 mM Tris-HCl buffer (pH 8.0), 0.15 M NaCl, 1 mM DTT and 10% glycerol.
Shipping: The product is shipped at ambient temperature. 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.
Otehr LCAD Enzymes:
Recombinant Human Long-chain specific acyl-CoA dehydrogenase mitochondrial
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