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EHHADH
Enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenaseECHD
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]
Top validated antibodies |
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| antibodies-online |  ABIN4880497 |
Monoclonal |
WB
EL
ICC
IHC
FC
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| OriGene | AM06711SU-N |
Monoclonal |
WB
EL
ICC
IHC
FC
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| LSBio | LS-C334238 |
Polyclonal |
WB
ICC
IHC
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| Proteintech Group | 26570-1-AP |
5 references | Polyclonal |
WB
EL
ICC
IHC
|
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| GeneTex | GTX81126 |
1 references | Polyclonal |
WB
IHC
FC
|
|
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