ALDH4A1 anticorps

N° du produit ABIN5696919

Cet anticorps anti-ALDH4A1 est un anticorps Lapin Polyclonal détectant ALDH4A1 dans WB, IHC, ELISA et IP. Adapté pour Humain, Souris et Rat.

Aperçu rapide pour ALDH4A1 anticorps (ABIN5696919)

Antigène: ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDH4A1 est non-conjugé

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

Détail du produit anti-ALDH4A1 anticorps

Fonction: ALDH4A1 antibody

Immunogène: aldehyde dehydrogenase 4 family, member A1

Isotype: IgG

Information d'application

Indications d'application: WB :1:500-1:5000,IHC:1:20-1:200,IP:1:200-1:2000

Commentaires:

human heart tissue were subjected to SDS PAGE followed by western blot with FNab00296(ALDH4A1 antibody) at dilution of 1:400

Restrictions: For Research Use only

Stockage

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

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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur ALDH4A1

Antigène: ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

Autre désignation: ALDH4A1

Sujet:

Synonyms: Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial (P5C dehydrogenase)|Aldehyde dehydrogenase family 4 member A1|L-glutamate gamma-semialdehyde dehydrogenase|ALDH4A1|ALDH4|P5CDH

Background: This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.

Poids moléculaire: 62kDa

ID gène: 8659

UniProt: P30038

Pathways: Monocarboxylic Acid Catabolic Process