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ALDH3A2 Mouse anti-Human, Clone: OTI1H10, liquid, TrueMAB™ Non-distribution product as customer accommodation.

Mouse Monoclonal Antibody

Manufacturer:  OriGeneSupplier Diversity Partner TA503143

Catalog No. 50-167-4109


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Description

Description

Aldh3A2 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes. Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Aldh3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome, an inherited neurocutaneous disorder. Patients with this disorder display ichthyosis, mental retardation and spastic diplegia. The pathogenesis of the cutaneous and neurological symptoms is thought to result from abnormal lipid accumulation in the membranes of skin and brain, the formation of aldehyde Schiff base adducts with amine-containing lipids or proteins, or defective eicosanoid metabolism.
Specifications

Specifications

ALDH3A2
Monoclonal
0.52 mg/mL
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide
P51648
ALDH10, FALDH, SLS
Mouse
IgG2b
100 μL
-20° C, Avoid Freeze/Thaw Cycles
Primary
224
Western Blot
OTI1H10
Unconjugated
ALDH3A2
Liquid
ALDH3A2
Full length human recombit protein of human ALDH3A2 produced in HEK293T cell.
Affinity Chromatography
RUO
Antibody
Monoclonal
Human
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