ALDH3A1 antibody

Catalog No. ABIN5696916

This anti-ALDH3A1 antibody is a Rabbit Polyclonal antibody detecting ALDH3A1 in WB, ELISA, IF and IP. Suitable for Human, Mouse and Rat.

Quick Overview for ALDH3A1 antibody (ABIN5696916)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ALDH3A1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)

Product Details anti-ALDH3A1 Antibody

Purpose: ALDH3A1 antibody

Immunogen: aldehyde dehydrogenase 3 family, memberA1

Isotype: IgG

Application Details

Application Notes: WB :1:1000-1:10000,IF:1:10-1:100,IP:1:500-1:5000

Comment:

HEK-293 cells were subjected to SDS PAGE followed by western blot with FNab00292(ALDH3A1 antibody) at dilution of 1:2000

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freeze / thaw cycles.

Storage: -20 °C

Storage Comment: -20°C for 12 months

Expiry Date: 12 months

Target Details for ALDH3A1

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

Alternative Name: ALDH3A1

Background:

Synonyms: Aldehyde dehydrogenase, dimeric NADP-preferring|ALDHIII|Aldehyde dehydrogenase 3|Aldehyde dehydrogenase family 3 member A1|ALDH3A1|ALDH3

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.

Molecular Weight: 50kDa

Gene ID: 218

UniProt: P30838