ALDH3A1 antibody (AA 62-101)

Catalog No. ABIN7876144

The Rabbit Polyclonal anti-ALDH3A1 antibody (ABIN7876144) specifically detects ALDH3A1 in WB, ELISA, IHC (p) and FACS. The antibody is reactive with Human samples.

Quick Overview for ALDH3A1 antibody (AA 62-101) (ABIN7876144)

Target: ALDH3A1 (Aldehyde Dehydrogenase 3 Family, Member A1 (ALDH3A1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ALDH3A1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Product Details anti-ALDH3A1 Antibody

Binding Specificity: AA 62-101

Purpose: ALDH3 Antibody / ALDH3A1 / Aldehyde dehydrogenase 3

Purification: Antigen affinity purified

Immunogen: Recombinant human protein (amino acids E62-H101) was used as the immunogen for the ALDH3 antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the ALDH3 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the ALDH3 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for ALDH3A1

Target: ALDH3A1 (Aldehyde Dehydrogenase 3 Family, Member A1 (ALDH3A1))

Alternative Name: ALDH3

Background: Aldehyde dehydrogenase, dimeric NADP-preferring is an enzyme that in humans is encoded by the ALDH3A1 gene. 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.

UniProt: P30838