ALDH5A1 Antikörper (AA 400-500)

Produktnummer ABIN7265542

Produktdetails anti-ALDH5A1 Antikörper

Target: ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))

Bindungsspezifität: AA 400-500

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ALDH5A1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Verwendungszweck: ALDH5A1 Rabbit pAb

Sequenz: VSKGATVVTG GKRHQLGKNF FEPTLLCNVT QDMLCTHEET FGPLAPVIKF DTEEEAIAIA NAADVGLAGY FYSQDPAQIW RVAEQLEVGM VGVNEGLISS V

Kreuzreaktivität: Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: A synthetic peptide corresponding to a sequence within amino acids 400-500 of human ALDH5A1 (NP_001071.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,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.

Lagerung: -20 °C

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

Details zu ALDH5A1

Target: ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))

Andere Bezeichnung: ALDH5A1 (ALDH5A1 Produkte)

Synonyme: SSADH antikoerper, SSDH antikoerper, Ssadh antikoerper, 6330403E24Rik antikoerper, Ahd-1 antikoerper, Ahd1 antikoerper, D630032B01Rik antikoerper, OTTMUSG00000000613 antikoerper, Ssdh1 antikoerper, aldehyde dehydrogenase 5 family member A1 antikoerper, aldehyde dehydrogenase 5 family, member A1 antikoerper, aldhehyde dehydrogenase family 5, subfamily A1 antikoerper, ALDH5A1 antikoerper, aldh5a1 antikoerper, Aldh5a1 antikoerper

Hintergrund: This protein belongs to the aldehyde dehydrogenase family of proteins. This gene encodes a mitochondrial NAD(+)-dependent succinic semialdehyde dehydrogenase. A deficiency of this enzyme, known as 4-hydroxybutyricaciduria, is a rare inborn error in the metabolism of the neurotransmitter 4-aminobutyric acid (GABA). In response to the defect, physiologic fluids from patients accumulate GHB, a compound with numerous neuromodulatory properties. Two transcript variants encoding distinct isoforms have been identified for this gene.,ALDH5A1,SSADH,SSDH,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Amino acid metabolism,Lipid Metabolism,Neuroscience,ALDH5A1

Molekulargewicht: 57kDa/58kDa

Gen-ID: 7915

UniProt: P51649

Pathways: Monocarboxylic Acid Catabolic Process