Background：The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.
仕様
Synonyms：3 hydroxyacyl CoA dehydrogenase,3,2 trans enoyl CoA isomerase,3-hydroxyacyl-CoA dehydrogenase,ECHD,ECHP,EHHADH,Enoyl Coenzyme A,hydratase/3 hydroxyacyl Coenzyme A dehydrogenase,L 3 hydroxyacyl CoA dehydrogenase,L bifunctional protein,peroxisomal,L PBE,LBFP,LBP,MGC120586,MS730,PBE,PBFE,Peroxisomal bifunctional enzyme,Peroxisomal enoyl CoA hydratase
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human EHHADH
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
Dilution：WB1：500 - 1：2000
Gene_ID（human）：1962
Swissprot：Q08426
Isotype：IgG
Research Areas：Cancer, Cardiovascular, Metabolism, Signal transduction
