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A1076

HADH Rabbit polyclonal antibody

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£152.00

SKU:
A1076
Additional Names:
HAD|HADH|HADH1|HADHSC|HCDH|HHF4|MSCHAD|SCHAD
Application:
ELISA, WB, IHC-P
Molecular Weight:
34kda
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Abclonal
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulation:
Unmodified
Sequence:
MAFVTRQFMRSVSSSSTASASAKKIIVKHVTVIGGGLMGAGIAQVAAATGHTVVLVDQTEDILAKSKKGIEESLRKVAKKKFAENPKAGDEFVEKTLSTIATSTDAASVVHSTDLVVEAIVENLKVKNELFKRLDKFAAEHTIFASNTSSLQITSIANATTRQDRFAGLHFFNPVPVMKLVEVIKTPMTSQKTFESLVDFSKALGKHPVSCKDTPGFIVNRLLVPYLMEAIRLYERGDASKEDIDTAMKLGAGYPMGPFELLDYVGLDTTKFIVDGWHEMDAENPLHQPSPSLNKLVAENKFGKKTGEGFYKYK
Uniprot:
Q16836
Synonyms:
HAD;HADH1;HADHSC;HCDH;HHF4;hydroxyacyl-coenzyme A dehydrogenase, mitochondrial;L-3-hydroxyacyl-Coenzyme A dehydrogenase, short chain;medium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase;MSCHAD;SCHAD;short-chain 3-hydroxyacyl-CoA dehydrogenase;testis secretory sperm-binding protein Li 203a
Extra Details:
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.
Shipping Conditions:
Blue Ice