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Antibody detects endogenous levels of total ACAD9.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: ACAD-9; Acyl-CoA dehydrogenase family member 9; acyl-CoA dehydrogenase family member 9, mitochondrial; acyl-CoA dehydrogenase family, member 9; acyl-Coenzyme A dehydrogenase family, member 9; Complex I assembly factor ACAD9, mitochondrial; very-long-chain acyl-CoA dehydrogenase VLCAD; very-long-chain acyl-CoA dehydrogenase VLCAD homolog
基因别名: 2600017P15Rik; 4732402K02; ACAD9; C630012L17Rik; NPD002; Nyggf2
UniProt ID: (Human) Q9H845, (Rat) B1WC61, (Mouse) Q8JZN5
Entrez Gene ID: (Human) 28976, (Rat) 294973, (Mouse) 229211