ALDH4A1 Antikörper

Produktnummer ABIN7235779

Produktdetails anti-ALDH4A1 Antikörper

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ALDH4A1 Antikörper ist unkonjugiert

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

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human ALDH4A1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, IHC 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.3 mg/mL

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu ALDH4A1

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

Andere Bezeichnung: ALDH4A1 (ALDH4A1 Produkte)

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

Hintergrund: 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.

Molekulargewicht: 62 kDa

UniProt: P30038

Pathways: Monocarboxylic Acid Catabolic Process