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ALDH3A2
Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Protein class
Disease related genes, Enzymes, Human disease related genes, Metabolic proteins, Potential drug targets
Predicted location
Intracellular, Membrane (different isoforms)
Single cell type specificity
Cell type enhanced (Basal squamous epithelial cells, Squamous epithelial cells)
Immune cell specificity
Low immune cell specificity
Cell line specificity
Cell line enhanced (OE19)
Interaction
Homodimer.
Molecular function
Oxidoreductase
More Types Infomation
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- Derivation: Phage display library screening
- Species Reactivity: Mouse, Human
- Type: Rabbit IgG
- Application: WB, IF, FC
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- Derivation: Mouse
- Species Reactivity: Human, Rat, Rabbit, Mouse
- Type: Mouse IgG2a
- Application: ELISA, WB
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- Derivation: Mouse
- Species Reactivity: Human, Mouse
- Type: Mouse IgG1, κ
- Application: WB, IHC-P
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- Species Reactivity: E. coli, Human, Mouse, Rat, Rabbit
- Type: Mouse IgG
- Application: WB
-
- Species Reactivity: Human
- Type: Mouse IgG
- Application: WB
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For Research Use Only. Not For Clinical Use.