ALDH3A1 anticorps

N° du produit ABIN7240436

Détail du produit anti-ALDH3A1 anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDH3A1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of human ALDH3A1

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.4 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur ALDH3A1

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

Autre désignation: ALDH3A1 (ALDH3A1 Produits)

Synonymes: anticorps ALDC, anticorps ALDH-E1, anticorps ALDH1, anticorps ALDH11, anticorps PUMB1, anticorps RALDH1, anticorps ALDH3, anticorps ALDHIII, anticorps Ahd-4, anticorps Ahd4, anticorps Aldh, anticorps Aldh3, anticorps AHDC, anticorps Ahd-c, anticorps aldehyde dehydrogenase 1 family member A1, anticorps aldehyde dehydrogenase 3 family member A1, anticorps aldehyde dehydrogenase, anticorps aldehyde dehydrogenase, dimeric NADP-preferring, anticorps aldehyde dehydrogenase family 3, subfamily A1, anticorps aldehyde dehydrogenase 3 family, member A1, anticorps ALDH1A1, anticorps ALDH3A1, anticorps OE_RS03630, anticorps LOC100077088, anticorps CLL_A1665, anticorps LOC100281700, anticorps LOC100285809, anticorps Aldh3a1

Sujet: 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.

Poids moléculaire: 50 kDa

UniProt: P30838