Human GBA1 (Lysosomal Acid Glucosylceramidase) - Recombinant Protein
Beta LifeScience
SKU/CAT #: BLT-01162P

SDS-PAGE analysis of Human GBA1 (Lysosomal Acid Glucosylceramidase) - Recombinant Protein, CAT# BLT-01162P, showing >85% purity under 15% SDS-PAGE (Reduced)
Human GBA1 (Lysosomal Acid Glucosylceramidase) - Recombinant Protein
Beta LifeScience
SKU/CAT #: BLT-01162P
Regular price
$59500
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Quantity Pricing
Pack Size | Price (USD) |
---|---|
500 µg | $1,030 (Fall Promotion) |
1 mg | $1,870 (Fall Promotion) |
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Product Overview
Product Name | Recombinant Human GBA (GBA1) Protein |
Product Overview | This recombinant human GBA (GBA1) protein includes amino acids 40-536aa of the target gene is expressed in Insect cell.The protein is supplied in lyophilized form and formulated in phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5% trehaloseprior to lyophilization. |
Target Uniprot Id | P04062 |
Recommended Name | Lysosomal acid glucosylceramidase |
Gene Name | GBA1 |
Synonyms | GBA1, GCB, GLUC |
Species | Human |
Predicted Molecular Mass | 56.4 kDa |
Expression System | Insect Cell |
Expression Range | 40-536aa |
Tag | N-6His |
Purity | >85% |
Formulation | Lyophilized |
Buffer | Phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5%Trehalose |
Storage Condition | 1. Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. 2. Avoid repeated freeze-thaw cycles. 3. Store working aliquots at 4°C for up to one week. 4. In general, protein in liquid form is stable for up to 6 months at -20°C/-80°C. Protein in lyophilized powder form is stable for up to 12 months at -20°C/-80°C. |
Reconstitution Instruction | Briefly centrifuged the vial prior to opening to bring the contents to the bottom. Reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL. It is recommended to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. The default final concentration of glycerol is 50%. |
Applications | Positive Control; Immunogen; SDS-PAGE; WB |
Research Area | Neuroscience |
Target Function | Glucosylceramidase that catalyzes, within the lysosomal compartment, the hydrolysis of glucosylceramide/GlcCer into free ceramide and glucose. Thereby, plays a central role in the degradation of complex lipids and the turnover of cellular membranes. Through the production of ceramides, participates in the PKC-activated salvage pathway of ceramide formation. Also plays a role in cholesterol metabolism. May either catalyze the glucosylation of cholesterol, through a transglucosylation reaction that transfers glucose from glucosylceramide to cholesterol. The short chain saturated C8:0-GlcCer and the mono-unsaturated C18:0-GlcCer being the most effective glucose donors for that transglucosylation reaction. Under specific conditions, may alternatively catalyze the reverse reaction, transferring glucose from cholesteryl-beta-D-glucoside to ceramide. Finally, may also hydrolyze cholesteryl-beta-D-glucoside to produce D-glucose and cholesterol. |
Subcellular Location | Lysosome membrane; Peripheral membrane protein; Lumenal side. |
Protein Family | Glycosyl hydrolase 30 family |
Associated Diseases | Gaucher disease (GD); Gaucher disease 1 (GD1); Gaucher disease 2 (GD2); Gaucher disease 3 (GD3); Gaucher disease 3C (GD3C); Gaucher disease perinatal lethal (GDPL); Parkinson disease (PARK) |