ALDH4A1 anticorps

N° du produit ABIN5696919

Cet anticorps anti-ALDH4A1 Polyclonal Lapin (ABIN5696919) détecte spécifiquement ALDH4A1 dans WB, IHC, ELISA et IP. L’anticorps est réactif avec des échantillons de 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