Background：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.
仕様
Synonyms：Acyl CoA dehydrogenase 9,Acyl Coenzyme A dehydrogenase family,member 9,acyl-CoA dehydrogenase family member 9,mitochondrial,FLJ23533,MGC14452,NPD002,Very long chain acyl CoA dehydrogenase VLCAD
Host：Rabbit
Reactivity：Human,Mouse
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human ACAD9
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
Dilution：WB 1：500 - 1：2000
Gene_ID（human）：28976
Swissprot：Q9H845
Isotype：IgG
Research Areas：Cancer, Metabolism, Signal transduction
