This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ACADMBA-20-REGO | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ACADMBA-20-REGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ACADMBA-20-ORGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ACADMBA-20-GOGR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ACADMBA-20-GRRE | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ACADMBA-20-GROR | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ACADMBA-20-GRGO | 20 (40 μL) | 200 μL |
|
Request Pricing |
| ACADMBA-20-AQOR | 20 (40 μL) | 200 μL |
|
Request Pricing |
This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : ACADM
Gene Name : Acyl-CoA dehydrogenase medium chain
Chromosome : CHR 1: 757,243,46-757,636,78
Locus : 1p31.1
Alt. Genes : LRPPRC
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.