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A5717

EHHADH Rabbit polyclonal antibody

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£152.00

SKU:
A5717
Additional Names:
ECHD|EHHADH|FRTS3|L-PBE|LBFP|LBP|MFE1|PBFE
Application:
ELISA, WB
Molecular Weight:
79kDa
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Abclonal
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulation:
Unmodified
Sequence:
EVIPSQYSSPTTIATVMNLSKKIKKIGVVVGNCFGFVGNRMLNPYYNQAYFLLEEGSKPEEVDQVLEEFGFKMGPFRVSDLAGLDVGWKSRKGQGLTGPTLLPGTPARKRGNRRYCPIPDVLCELGRFGQKTGKGWYQYDKPLGRIHKPDPWLSKFLSRYRKTHHIEPRTISQDEILERCLYSLINEAFRILGEGIAASPEHIDVVYLHGYGWPRHKGGPMFYASTVGLPTVLEKLQKYYRQNPDIPQLEPSDYLKKLASQGNPPLKEWQSLAGSPSSKL
Uniprot:
Q08426
Synonyms:
3,2-trans-enoyl-CoA isomerase;ECHD;enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase;enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase;FRTS3;L-3-hydroxyacyl-CoA dehydrogenase;L-bifunctional protein, peroxisomal;L-PBE;LBFP;LBP;MFE1;multifunctional enzyme 1;PBE;PBFE;peroxisomal bifunctional enzyme;peroxisomal enoyl-CoA hydratase
Extra Details:
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.
Shipping Conditions:
Blue Ice