Background：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.
仕様
Synonyms：ACAD4,ACADL,ACADL,Acyl Coenzyme A dehydrogenase long chain,Acyl-CoA dehydrogenase long chain,FLJ94052 ,LCAD,Long chain acyl CoA dehydrogenase,Long-chain specific acyl-CoA dehydrogenase, mitochondrial
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human ACADL
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）：33
Swissprot：P28330
Isotype：IgG
Research Areas：Cancer, Cardiovascular, Metabolism, Signal transduction
