HADH Antilichaam

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.

3033

Q16836

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-314 of human HADH (NP_005318.3) .

Unconjugated

Primary Antibodies

Cancer, Signal Transduction

Affinity purification

HepG2

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 34kDa

IgG

HADH

Mouse kidney

Mouse pancreas

Rat kidney

Rat liver

Hydroxyacyl-CoA dehydrogenase

Homo sapiens

HADH, HAD, HADH1, HADHSC, HHF4, M/SCHAD, MGC8392, SCHAD, HCDH, MSCHAD

WB, IHC

Liquid