Short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD)


UniProt Number: Q16836
Alternate Names: Medium and short chain L-3-hydroxyacyl-coenzyme A dehydrogenase, hydroxyacyl-coenzyme A dehydrogenase, HCDH, HADH, HADHSC
Structure and Function: Plays an essential role in the mitochondrial beta-oxidation of short chain fatty acids. Exerts its highest activity toward 3-hydroxybutyryl-CoA.
Disease Associations: Defects in HADH are the cause of 3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] and familial hyperinsulinemic hypoglycemia type 4 (HHF4) [MIM:609975]; also known as persistent hyperinsulinemic hypoglycemia of infancy (PHHI) or congenital hyperinsulinism.



Monoclonal Antibodies
Cat. No. Name Reactivity Apps. Amount Price  
MS706 SCHAD antibody human ICC, IHC, IP, ICE 100 µg $325.00


Protein Quantity Assays
Cat. No. Name Reactivity Amount Price  
MSFX-10 SCHAD FlexPlex™ Module human 4 strips (32 tests) $125.00


Multiplexing Arrays
Cat. No. Name Reactivity Amount Price  
MSX32 MetaPath™ Fatty Acid Oxdiation 4-Plex Dipstick Array human 30 tests $545.00
90 tests $995.00



Browse Products By:
Product Search:


Product Finder Tool   


Related Pathways:



Fatty Acid Oxidation (Mitochondrial)


Subscribe to MitoNews
MitoNews is a free periodic annotated review of important publications in mitochondria and metabolic research.

Sales & Customer Support:
1-800-910-6486

[email protected]

Copyright © 2010 MitoSciences Inc. All rights reserved.