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EHHADH


Official Full Name
enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
Organism
Homo sapiens
Gene ID
1962
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. [provided by RefSeq, Oct 2009]
Synonyms
LBP; ECHD; LBFP; MFE1; PBFE; FRTS3; L-PBE

Cat.No. Product Name Price
SHH027785 shRNA set against Rat Ehhadh(NM_133606.1) Inquiry
SHH284037 shRNA set against Mouse EHHADH (NM_023737.3) Inquiry
SHH284041 shRNA set against Rat EHHADH (NM_133606.1) Inquiry
SHW017686 shRNA set against Danio rerio EHHADH (NM_207068) Inquiry
Cat.No. Product Name Price
CDCB157862 Human EHHADH ORF clone (BC038948) Inquiry
CDFR014118 Rat Ehhadh cDNA Clone(NM_133606.1) Inquiry
MiUTR1R-01677 EHHADH miRNA 3'UTR clone Inquiry
CDCB179161 Danio rerio EHHADH ORF Clone (NM_207068) Inquiry
CDCH017328 Mouse EHHADH ORF clone(NM_023737.3) Inquiry
CDCR381173 Rat Ehhadh ORF Clone(NM_133606.1) Inquiry
CDCS408845 Human EHHADH ORF Clone (BC038948) Inquiry
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