| Product Name | ALDH3A1 Antibody |
|---|---|
| Description | Rabbit polyclonal antibody to ALDH3A1 |
| Synonyms | Acetaldehyde dehydrogenase 3 antibody; AHD 4 antibody; AHD C antibody; AHD4 antibody; AHDC antibody; AL3A1_HUMAN antibody; Aldehyde dehydrogenase 3 antibody; Aldehyde dehydrogenase 3 family member A1 antibody; Aldehyde dehydrogenase 3A1 antibody; Aldehyde dehydrogenase antibody; Aldehyde dehydrogenase class 3 antibody; Aldehyde dehydrogenase dimeric NADP preferring antibody; Aldehyde dehydrogenase family 3 member A1 antibody; Aldehyde dehydrogenase family 3 subfamily A1 antibody; Aldehyde dehydrogenase family 3, subfamily A, member 1 antibody; Aldehyde dehydrogenase isozyme 3 antibody; Aldehyde dehydrogenase type III antibody; ALDH 3 antibody; ALDH 3A1 antibody; ALDH III antibody; ALDH, stomach type antibody; ALDH3 A1 antibody; ALDH3 antibody; ALDH3A 1 antibody; Aldh3a1 antibody; ALDHIII antibody; dimeric NADP-preferring antibody; MGC10406 antibody; Stomach aldehyde dehydrogenase antibody; Tumor associated aldehyde dehydrogenase tumor ALDH antibody |
| Host | Rabbit |
| Clonality | Polyclonal |
| Conjugate | Unconjugated |
| Immunogen | Fusion protein of human ALDH3A1 |
| Isotype | IgG |
| Target | ALDH3A1 |
| Reactivity | Human, Mouse, Rat |
| Applications | ELISA, IHC, WB |
| Form | Liquid |
| Diluent Buffer | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Uniprot | P30838 |
| Storage | Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. |
| Background | Aldehyde dehydrogenases oxidize various aldehydes to the corresponding acids. They are involved in the detoxification of alcohol-derived acetaldehyde and in the metabolism of corticosteroids, biogenic amines, neurotransmitters, and lipid peroxidation. The enzyme encoded by this gene forms a cytoplasmic homodimer that preferentially oxidizes aromatic and medium-chain (6 carbons or more) saturated and unsaturated aldehyde substrates. It is thought to promote resistance to UV and 4-hydroxy-2-nonenal-induced oxidative damage in the cornea. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Multiple alternatively spliced variants, encoding the same protein, have been identified. |
| Supplier | Cusabio |
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