EHHADH polyclonal, anti-human antibody
€305.00
In stock
SKU
AC-ABV11229-100
Catalog Number: AC-ABV11229-100
Size: 100 µg
Host: Rabbit IgG
Applications: WB
Datasheet
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Size: 100 µg
Host: Rabbit IgG
Applications: WB
Datasheet
Request Information
Background:
EHHADH is a bifunctional enzyme. It is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of this 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. EHHADH-null mice only exhibit a blunted peroxisome proliferative response when challenged with a peroxisome proliferator.
Other Names:
Enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase, LBFP, LBP, L-PBE, peroxisomal bifunctional enzyme3, 2-trans-enoyl-CoA isomerase, peroxisomal enoyl-CoA hydratase
Primary Accession: Q08426
Gene Name: EHHADH (HGNC:3247)
Gene ID: 1962
Concentration (mg/ml): 0.5 mg/ml
EHHADH is a bifunctional enzyme. It is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of this 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. EHHADH-null mice only exhibit a blunted peroxisome proliferative response when challenged with a peroxisome proliferator.
Other Names:
Enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase, LBFP, LBP, L-PBE, peroxisomal bifunctional enzyme3, 2-trans-enoyl-CoA isomerase, peroxisomal enoyl-CoA hydratase
Primary Accession: Q08426
Gene Name: EHHADH (HGNC:3247)
Gene ID: 1962
Concentration (mg/ml): 0.5 mg/ml
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