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Invitrogen
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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: HCDH; Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial; M/SCHAD; Medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase; MGC8392; Short-chain 3-hydroxyacyl-CoA dehydrogenase
基因别名: HAD; HAD1; HADH; HADHSC; SCHAD
Entrez Gene ID: (Human) 3033