GBA Antikörper

Produktnummer ABIN7267407

Produktdetails anti-GBA Antikörper

Target: GBA (Glucosidase, Beta, Acid (GBA))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser GBA Antikörper ist unkonjugiert

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

Verwendungszweck: Glucosylceramidase beta (GBA) Rabbit mAb

Kreuzreaktivität: Human, Ratte

Produktmerkmale: Monoclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: A synthesized peptide derived from human Glucosylceramidase beta (Glucosylceramidase beta (GBA))

Isotyp: IgG

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,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 GBA

Target: GBA (Glucosidase, Beta, Acid (GBA))

Andere Bezeichnung: GBA (GBA Produkte)

Synonyme: GBA1 antikoerper, GCB antikoerper, GLUC antikoerper, BETA-GLUCOSIDASE antikoerper, T12J13.8 antikoerper, T12J13_8 antikoerper, beta glucosidase 25 antikoerper, PSPTO3318 antikoerper, PSPTO4290 antikoerper, GC antikoerper, GCase antikoerper, betaGC antikoerper, glucosylceramidase beta antikoerper, beta glucosidase 25 antikoerper, beta-glucosidase antikoerper, Beta-glucosidase antikoerper, glucosidase, beta, acid antikoerper, glucosylceramidase antikoerper, bglX-2 antikoerper, GBA antikoerper, BGLU25 antikoerper, PSPTO_3318 antikoerper, bglX antikoerper, bglA4 antikoerper, Gba antikoerper, LOC100399524 antikoerper, bglA.2 antikoerper, bglX-2 antikoerper

Hintergrund: This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2010],GBA,GBA1,GCB,GLUC,Cancer,Cell Type Marker,Cell Type Marker_Oligodendrocyte marker,Endocrine & Metabolism,Lipid Metabolism,Neurodegenerative Diseases,Neurodegenerative Diseases_Dopamine Signaling in Parkinsons Disease,Neuroscience,Signal Transduction,GBA

Molekulargewicht: 60kDa

Gen-ID: 2629

UniProt: P04062

Pathways: Cellular Glucan Metabolic Process