|ELISA (ELISA)||Assay Dependent|
|Immunocytochemistry (ICC)||5 ug/ml|
|Immunohistochemistry (IHC)||Assay Dependent|
|Immunoprecipitation (IP)||Assay Dependent|
|Tested Species reactivity||Human|
|Host / Isotype||Mouse / IgG1|
|Immunogen||Human liver mitochondria|
|Storage buffer||HEPES buffered saline|
|Contains||0.02% sodium azide|
|Storage conditions||4° C|
This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: HADH1; HADHSC; HCDH; HHF4; hydroxyacyl-coenzyme A dehydrogenase; Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial; L-3-hydroxyacyl-Coenzyme A dehydrogenase; L-3-hydroxyacyl-Coenzyme A dehydrogenase, short chain; Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase; mitochondrial; MSCHAD; SCHAD; short chain; Short-chain 3-hydroxyacyl-CoA dehydrogenase; testis secretory sperm-binding protein Li 203a
Gene Aliases: HAD; HADH; HADH1; HADHSC; HCDH; HHF4; MSCHAD; SCHAD
UniProt ID: (Human) Q16836
Entrez Gene ID: (Human) 3033
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