ALDH7A1 Antikörper

Produktnummer ABIN7264665

Produktdetails anti-ALDH7A1 Antikörper

Target: ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ALDH7A1 Antikörper ist unkonjugiert

Applikation: Immunofluorescence (IF)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human ALDH7A1 (NP_001173.2).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF 1:50-1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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 ALDH7A1

Target: ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

Andere Bezeichnung: ALDH7A1 (ALDH7A1 Produkte)

Synonyme: atq1 antikoerper, ALDH7A1 antikoerper, ATQ1 antikoerper, EPD antikoerper, PDE antikoerper, antiquitin antikoerper, ATQ antikoerper, wu:fi34d12 antikoerper, wu:fi35e06 antikoerper, Atq1 antikoerper, D18Wsu181e antikoerper, aldehyde dehydrogenase 7 family member A1 antikoerper, aldehyde dehydrogenase 7 family member A1 L homeolog antikoerper, aldehyde dehydrogenase 7 family, member A1 antikoerper, aldehyde dehydrogenase family 7, member A1 antikoerper, ALDH7A1 antikoerper, aldh7a1 antikoerper, aldh7a1.L antikoerper, Aldh7a1 antikoerper

Hintergrund: The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family. These enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular member has homology to a previously described protein from the green garden pea, the 26g pea turgor protein. It is also involved in lysine catabolism that is known to occur in the mitochondrial matrix. Recent reports show that this protein is found both in the cytosol and the mitochondria, and the two forms likely arise from the use of alternative translation initiation sites. An additional variant encoding a different isoform has also been found for this gene. Mutations in this gene are associated with pyridoxine-dependent epilepsy. Several related pseudogenes have also been identified.

Gen-ID: 501

UniProt: P49419

Pathways: Sensory Perception of Sound