The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ACADLBA-20-REGO | 20 (40 μL) | 200 μL |
|
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| ACADLBA-20-REGR | 20 (40 μL) | 200 μL |
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| ACADLBA-20-ORGR | 20 (40 μL) | 200 μL |
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| ACADLBA-20-GOGR | 20 (40 μL) | 200 μL |
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| ACADLBA-20-GRRE | 20 (40 μL) | 200 μL |
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| ACADLBA-20-GROR | 20 (40 μL) | 200 μL |
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| ACADLBA-20-GRGO | 20 (40 μL) | 200 μL |
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| ACADLBA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [provided by RefSeq, Jul 2008]
Gene Symbol : ACADL
Gene Name : Acyl-CoA dehydrogenase long chain
Chromosome : CHR 2: 210,225,490-210,187,989
Locus : 2q34
Alt. Genes : LRPPRC
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