Glucosidase, beta Antikörper (AA 352-529)

Produktnummer ABIN1886398

Produktdetails anti-Glucosidase, beta Antikörper

Target: Glucosidase, beta

Bindungsspezifität: AA 352-529

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Glucosidase, beta Antikörper ist unkonjugiert

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

Aufreinigung: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 352 and 529 of Human GBA

Anwendungsinformationen

Applikationshinweise: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.250
Immunofluorescence: 1.100-1.200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Konservierungsmittel: Thimerosal (Merthiolate)

Vorsichtsmaßnahmen: Biohazard Informations: This product contains thimerosal which is hazardous.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Details zu Glucosidase, beta

Target: Glucosidase, beta

Andere Bezeichnung: beta-glucosidase (Glucosidase, beta Produkte)

Synonyme: BETA-GLUCOSIDASE antikoerper, GLUC antikoerper, T12J13.8 antikoerper, T12J13_8 antikoerper, beta glucosidase 25 antikoerper, PSPTO3318 antikoerper, PSPTO4290 antikoerper, beta glucosidase 25 antikoerper, beta-glucosidase antikoerper, Beta-glucosidase antikoerper, glucosylceramidase antikoerper, bglX-2 antikoerper, BGLU25 antikoerper, PSPTO_3318 antikoerper, bglX antikoerper, bglA4 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 encoding the same protein.[provided by RefSeq]

Molekulargewicht: 60 kDa

Gen-ID: 2629

NCBI Accession: NP_001005750, NM_001005750