ALDH3A2 anticorps (C-Term)

N° du produit ABIN499265

L’anticorps Lapin Polyclonal anti-ALDH3A2 a été validé pour WB et EIA. Il convient pour détecter ALDH3A2 dans des échantillons de Humain et Souris.

Aperçu rapide pour ALDH3A2 anticorps (C-Term) (ABIN499265)

Antigène: ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDH3A2 est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-ALDH3A2 anticorps

Épitope: C-Term

Specificité: This antibody reacts to ALDH3A2.

Purification: Affinity chromatography purified via peptide column

Immunogène: Aldh3A2 antibody was raised against a 14 amino acid peptide near the carboxy terminus of the human Aldh3A2.

Isotype: IgG

Information d'application

Indications d'application: ELISA. Western Blot: Aldh3A2 antibody can be used for detection of Aldh3A2 at 1 - 2 μg/mL.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Buffer: PBS containing 0.02 % sodium azide.

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: 4 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C.

Détails sur ALDH3A2

Antigène: ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))

Autre désignation: ALDH3A2 / ALDH10

Sujet: Aldh3A2 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes. Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Aldh3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome, an inherited neurocutaneous disorder. Patients with this disorder display ichthyosis, mental retardation and spastic diplegia. The pathogenesis of the cutaneous and neurological symptoms is thought to result from abnormal lipid accumulation in the membranes of skin and brain, the formation of aldehyde Schiff base adducts with amine-containing lipids or proteins, or defective eicosanoid metabolism. At least four isoforms of Aldh3A2 are known to exist. This antibody is predicted to have no cross-reactivity to Aldh3A1.Synonyms: Aldehyde dehydrogenase 10, Aldehyde dehydrogenase family 3 member A2, FALDH, Fatty aldehyde dehydrogenase, Microsomal aldehyde dehydrogenase

ID gène: 224

NCBI Accession: NP_001026976

UniProt: P51648