GALT Antikörper

Produktnummer ABIN2430153

Produktdetails anti-GALT Antikörper

Target: GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GALT Antikörper ist unkonjugiert

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

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human GALT

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

Handhabung: Avoid freeze / thaw cycles.

Lagerung: -20 °C

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

Details zu GALT

Target: GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))

Andere Bezeichnung: GALT (GALT Produkte)

Synonyme: GALT antikoerper, AW553376 antikoerper, CG9232 antikoerper, Dmel\\CG9232 antikoerper, dGALT antikoerper, galactose-1-phosphate uridylyltransferase antikoerper, galactose-1-phosphate uridylyltransferase, GalT antikoerper, probable galactose-1-phosphate uridylyltransferase galtb [second part] antikoerper, UDP-glucose--galactose-1-phosphate uridylyltransferase antikoerper, GalT galactose-1-phosphate uridylyltransferase antikoerper, galactose-1-phosphate uridyl transferase antikoerper, Galactose-1-phosphate uridylyltransferase antikoerper, galactose-1-phosphate uridylyltransferase S homeolog antikoerper, GALT antikoerper, galT antikoerper, Galt antikoerper, CNM00620 antikoerper, Mrub_2813 antikoerper, Mesil_2395 antikoerper, Trad_0989 antikoerper, Igag_1846 antikoerper, VDIS_RS10425 antikoerper, Intca_2810 antikoerper, Marky_2157 antikoerper, Selsp_1876 antikoerper, Trebr_2368 antikoerper, Halhy_5538 antikoerper, Theth_1357 antikoerper, galt.S antikoerper

Hintergrund: Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht: Calculated MW: 43 kDa

NCBI Accession: NP_000146