ALDH4A1 anticorps

N° du produit ABIN7235779

Détail du produit anti-ALDH4A1 anticorps

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

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of human ALDH4A1

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: 0.3 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 ALDH4A1

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

Autre désignation: ALDH4A1 (ALDH4A1 Produits)

Synonymes: anticorps aldh4, anticorps p5cd, anticorps p5cdh, anticorps ALDH4, anticorps P5CD, anticorps P5CDh, anticorps A930035F14Rik, anticorps Ahd-1, anticorps Ahd1, anticorps Aldh4, anticorps Aldh5a1, anticorps E330022C09, anticorps P5cd, anticorps P5cdh, anticorps P5cdhl, anticorps P5cdhs, anticorps Ssdh1, anticorps zgc:63592, anticorps aldehyde dehydrogenase 4 family member A1, anticorps aldehyde dehydrogenase 4 family, member A1, anticorps aldehyde dehydrogenase 4 family member A1 L homeolog, anticorps aldh4a1, anticorps ALDH4A1, anticorps Aldh4a1, anticorps aldh4a1.L

Sujet: 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: 62 kDa

UniProt: P30038

Pathways: Monocarboxylic Acid Catabolic Process