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Key Documents

HPA039588

Sigma-Aldrich

Anti-HADH antibody produced in rabbit

affinity isolated antibody, buffered aqueous glycerol solution

Synonym(s):

Anti-HADH1, Anti-HADHSC, Anti-Hydroxyacyl-CoA dehydrogenase, Anti-SCHAD

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About This Item

UNSPSC Code:
12352203
Human Protein Atlas Number:
NACRES:
NA.41

biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous glycerol solution

species reactivity

human

technique(s)

immunoblotting: 0.04-0.4 μg/mL
immunohistochemistry: 1:1000-1:2500

immunogen sequence

YLMEAIRLYERGDASKEDIDTAMKLGAGYPMGPFELLDYVGLDTTKFIVDGWHEMDAENPLHQPSPSLNKLVAENKFGKKTGEGFY

UniProt accession no.

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... HADH(3033)

General description

Hydroxyacyl-coenzyme A dehydrogenase (HADH), also called short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD), is a 34 kDa protein expressed in heart, liver, kidney, pancreas and skeletal muscle. HADH is located on human chromosome 4q25. HADH has a N-terminal NAD+ binding domain and a C-terminal domain for dimerization and harbors a mitochondrial specific signal peptide.

Immunogen

hydroxyacyl-CoA dehydrogenase recombinant protein epitope signature tag (PrEST)

Application

All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project and as a result, are supported by the most extensive characterization in the industry.

The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. We also provide Prestige Antibodies® protocols and other useful information.

Biochem/physiol Actions

Hydroxyacyl-coenzyme A dehydrogenase (HADH) catalyses the conversion of L-3-hydroxyacyl-CoA to 3-ketoacyl-CoA, in the presence of NAD+ in mitochondria. The C-terminal domain interacts with substrate and is crucial for its activity. Mutation in the HADH gene elevates 3-hydroxyglutarate levels, leading to hyperinsulinism and hypoglycemia. Mutations in HADH gene is also implicated in short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency and may also contribute to the pathogenesis of neuronal disorders.

Features and Benefits

Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

Every Prestige Antibody is tested in the following ways:
  • IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
  • Protein array of 364 human recombinant protein fragments.

Linkage

Corresponding Antigen APREST79766

Physical form

Solution in phosphate buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide.

Legal Information

Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Diagnosis of ABCC8 Congenital Hyperinsulinism of Infancy in a 20-Year-Old Man Evaluated for Factitious Hypoglycemia
Gutgold A, et al.
The Journal of Clinical Endocrinology and Metabolism, 102(2), 345-349 (2016)
3-Hydroxyacyl-CoA dehydrogenase and short chain 3-hydroxyacyl-CoA dehydrogenase in human health and disease
Yang SY, et al.
FEBS Journal, 272(19), 4874-4883 (2005)
Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion
Clayton PT, et al.
The Journal of Clinical Investigation, 108(3), 457-465 (2001)
Human short-chain L-3-hydroxyacyl-CoA dehydrogenase: cloning and characterization of the coding sequence
Vredendaal P, et al.
Biochemical and Biophysical Research Communications, 223(3), 718-723 (1996)
Sequestration of the Active Site by Interdomain Shifting CRYSTALLOGRAPHIC AND SPECTROSCOPIC EVIDENCE FOR DISTINCT CONFORMATIONS OF l-3-HYDROXYACYL-CoA DEHYDROGENASE
Barycki JJ, et al.
The Journal of Clinical Endocrinology and Metabolism, 275(35), 27186-27196 (2000)

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