Recombinant Human Cytosolic beta-Glucosidase/GBA3, CF Summary
Details of Functionality
Measured by its ability to hydrolyze 4-methylumbelliferyl-beta -D-glucopyranoside. The specific activity is >1,500 pmol/min/μg, as measured under the described conditions.
Source
Spodoptera frugiperda, Sf 21 (baculovirus)-derived human Cytosolic beta-Glucosidase/GBA3 protein Thr13-Leu469 with a C-terminal 6-His tag
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Enzyme Activity
Theoretical MW
53 kDa & 41 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
54 kDa, reducing conditions
Publications
Read Publication using 5969-GH in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
6 months from date of receipt, -70 °C as supplied.
3 months, -70 °C under sterile conditions after opening.
Buffer
Supplied as a 0.2 μm filtered solution in Tris, NaCl, DTT and Glycerol.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Assay Procedure
Assay Buffer: 0.1 M MES, pH 6.5
Recombinant Human Cytosolic beta ‑Glucosidase/GBA3 (rhGBA3) (Catalog # 5969-GH)
Substrate: 4-methylumbelliferyl-beta -D-glucopyranoside (Sigma, Catalog # M3633), 10 mM stock in DMSO
F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
Dilute rhGBA3 to 1 ng/μL in Assay Buffer.
Dilute Substrate to 800 μM in Assay Buffer.
Load in a plate 50 μL of 1 ng/μL rhGBA3, and start the reaction by adding 50 μL of 800 μM Substrate. Include a control containing 50 μL of Assay Buffer and 50 μL of 800 μM Substrate.
Read at excitation and emission wavelengths of 365 nm and 445 nm (top read), respectively, in kinetic mode for 5 minutes.
Calculate specific activity:
Specific Activity (pmol/min/µg) =
Adjusted Vmax* (RFU/min) x Conversion Factor** (pmol/RFU)
amount of enzyme (µg)
*Adjusted for Substrate Blank **Derived using calibration standard 4-methylumbelliferone (Sigma, Catalog # M1381).
Per Well:
rhGBA3: 0.050 μg
Substrate: 400 μM
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Cytosolic beta-Glucosidase/GBA3, CF
CBG
CBGL1
CBGL1GLUC
Cytosolic betaGlucosidase
Cytosolic beta-Glucosidase
Cytosolic beta-glucosidase-like protein 1
EC 3.2.1.21
GBA3
GLUC
glucosidase, beta, acid 3 (cytosolic)
klotho-related protein
KLrP
MGC104276
MGC126878
Background
There are three beta ‑glucosidases (GBA) in human genome. GBA1 endodes a lysosomal membrane protein that cleaves the beta ‑glucosidic linkage of glucosylceramide (1). GBA2 encodes a microsomal beta ‑glucosidase that catalyzes the hydrolysis of bile acid 3-O-glucosides (2). GBA3 is a cytosolic beta ‑Glucosidase and is predominantly expressed in liver. GBA3 efficiently hydrolyzes beta ‑D‑glucoside and beta ‑D‑galactoside, but not any known physiological beta ‑glycoside, suggesting that it may be involved in detoxification of plant glycosides (3). GBA3 also has significant neutral glycosylceramidase activity, suggesting that it may be involved in a nonlysosomal catabolic pathway of glucosylceramide metabolism (4). At the protein level, GBA3 shows significant homology (>40%) with Klotho protein that is known for its association with aging process (3, 4).
Tybulewicz, V.L. et al. (1992) Nature 357:407.
Matern, H. et al. (2001) J. Biol. Chem. 276:37929.
de Graaf, M. et al. (2001) Biochem. J. 356:907.
Hayashi, Y. et al. (2007) J. Biol. Chem. 282:30889.
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