ALDH4A1 Antikörper

Produktnummer ABIN5696919

Der Kaninchen Polyklonal anti-ALDH4A1 Antikörper (ABIN5696919) detektiert spezifisch ALDH4A1 in WB, IHC, ELISA und IP. Dieser Antikörper reagiert spezifisch mit Proben aus Human, Maus und Ratte.

Kurzübersicht für ALDH4A1 Antikörper (ABIN5696919)

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, Immunoprecipitation (IP)

Produktdetails anti-ALDH4A1 Antikörper

Verwendungszweck: ALDH4A1 antibody

Immunogen: aldehyde dehydrogenase 4 family, member A1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB :1:500-1:5000,IHC:1:20-1:200,IP:1:200-1:2000

Kommentare:

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freeze / thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: -20°C for 12 months

Haltbarkeit: 12 months

Details zu ALDH4A1

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

Andere Bezeichnung: ALDH4A1

Hintergrund:

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.

Molekulargewicht: 62kDa

Gen-ID: 8659

UniProt: P30038

Pathways: Monocarboxylic Acid Catabolic Process