Product Description

GBA Rabbit Monoclonal Antibody

Sizes: 50μl, 100μl

Catalogue Numbers: BS40462-50, BS40462-100

Lead times: 1-2 weeks, if manufacturer has product in stock

Manufacturer/Ship Location: China

Background: Defects in GBA are the cause of Gaucher disease (GD) [MIM:230800], also known as glucocerebrosidase deficiency. GD is the most prevalent lysosomal storage disease, characterized by accumμlation of glucosylceramide in the reticμlo-endothelial system.

Category: Primary Antibody

Reactivity: Human Rat

Host: Rabbit

Applications: WB, IHC

Alternate Names: Alglucerase, betaGC, GBA1, GCase, GCB, GLUC, Glucosylceramidase, Imiglucerase,

Clonality: Monoclonal

Conjugate: Unconjugated

Modification: Unmodified

Immunogen: A synthesized peptide derived from human GBA

Dilution: WB 1:500~1:2000 IHC 1:50~1:200

Purification: Affinity-chromatography

Specificity: GBA Antibody detects endogenous levels of total GBA

Molecular Weight: 60kDa

Storage and Stability: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

SwissProt: P04062

Product: Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2.

Research Use Only