This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ACAD9-20-RE | 20 (40 μL) | 200 μL |  |
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| ACAD9-20-OR | 20 (40 μL) | 200 μL |  |
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| ACAD9-20-GO | 20 (40 μL) | 200 μL |  |
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| ACAD9-20-GR | 20 (40 μL) | 200 μL |  |
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| ACAD9-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
Gene Symbol : ACAD9
Gene Name : Acyl-CoA dehydrogenase family member 9
Chromosome : CHR 3: 128,879,489-128,916,074
Locus : 3q21.3
Alt. Genes : LRPPRC
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