Browse our anti-EHHADH (EHHADH) Antibodies

Full name:: anti-Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase Antibodies (EHHADH)

On www.antibodies-online.com are 73 Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH) Antibodies from 18 different suppliers available. Additionally we are shipping EHHADH Proteins (5) and EHHADH Kits (2) and many more products for this protein. A total of 86 EHHADH products are currently listed.

Synonyms:: 1, 1300002P22Rik, ECHD, Ehhadh, HD, L-PBE, LBFP, Lbp, MEF, Mfe, Mfe1, MFP, MFP1, Pbe, Pbfe, perMFE-1, zgc:77526

list all antibodies	Gene Name	GeneID	UniProt
	EHHADH	1962	Q08426 , Q9NY65
	EHHADH	171142	P07896
	EHHADH	74147	Q9DBM2
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Most Popular Reactivities for anti-EHHADH (EHHADH) Antibodies

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anti-Human EHHADH Antibodies:

anti-Rat (Rattus) EHHADH Antibodies:

21 WB Antibodies

anti-Mouse (Murine) EHHADH Antibodies:

26 WB Antibodies

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Relevant Pathways for anti-EHHADH Antibodies

Monocarboxylic Acid Catabolic Process

More product categories related to EHHADH Antibody

More Antibodies against EHHADH Interaction Partners

Human Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH) interaction partners

Mistargeting of peroxisomal EHHADH disrupts mitochondrial metabolism and leads to renal Fanconi's syndrome; this indicates a central role of mitochondria in proximal tubular function.

Mouse (Murine) Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH) interaction partners

The Ehhadh is indispensable for the production of medium-chain dicarboxylic acids, providing an explanation for the coordinated induction of mitochondrial and peroxisomal oxidative pathways during fasting.
bile acid biosynthesis, estimated by the ratio of C27/C24-bile acids, is more severely affected in double knock-out mice as compared with DBP (show GC Antibodies)-/- mice but was normal in LBP (show LBP Antibodies)-/- mice

EHHADH Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with EHHADH

enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase (EHHADH) antibody
enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase (ehhadh) antibody
enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase (Ehhadh) antibody
enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase (Ehhadh) antibody
peroxisomal bifunctional enzyme-like (LOC100135519) antibody

1 antibody
1300002P22Rik antibody
ECHD antibody
Ehhadh antibody
HD antibody
L-PBE antibody
LBFP antibody
Lbp antibody
MEF antibody
Mfe antibody
Mfe1 antibody
MFP antibody
MFP1 antibody
Pbe antibody
Pbfe antibody
perMFE-1 antibody
zgc:77526 antibody

Protein level used designations for EHHADH

enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase , peroxisomal bifunctional enzyme , 3,2-trans-enoyl-CoA isomerase , L-3-hydroxyacyl-CoA dehydrogenase , L-bifunctional protein, peroxisomal , PBE , peroxisomal enoyl-CoA hydratase , L-specific bifunctional protein , multifunctional enzyme type 1 , peroxisomal bifunctional enzyme type 1 , L-bifunctional enzyme , L-specific multifunctional beta-oxdiation protein , DKEYP-30D5.2 , PBFE , 2-enoylacyl-CoA hydratase , 3-hydroxyacyl-CoA dehydrogenase , enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase bifunctional enzyme

GENE ID	SPECIES
100067714	Equus caballus
460996	Pan troglodytes
701193	Macaca mulatta
100216115	Xenopus (Silurana) tropicalis
1962	Homo sapiens
171142	Rattus norvegicus
488110	Canis lupus familiaris
518852	Bos taurus
74147	Mus musculus
100000859	Danio rerio
100135519	Cavia porcellus

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