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| Catalog No. | Product Name | Size | List Price (US$) | Quantity |
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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.
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
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-C811: Recombinant Human Long-chain specific acyl-CoA dehydrogenase mitochondrial
Source: HEK 293-derived.
Purity > 95%, by reducing SDS-PAGE.
Endotoxin: Less than 0.1 ng/ug (1 EU/ug).
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.
Other LCAD Enzymes:
Recombinant Human Long-chain specific acyl-CoA dehydrogenase mitochondrial
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