Recombinant Human Arginase 1/ARG1 Protein, CF
R&D Systems | Catalog # 5868-AR
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Key Product Details
- R&D Systems E. coli-derived Recombinant Human Arginase 1/ARG1 Protein (5868-AR)
- Quality control testing to verify active proteins with lot specific assays by in-house scientists
- All R&D Systems proteins are covered with a 100% guarantee
Source
E. coli
Accession Number
Structure / Form
Monomer
Applications
Enzyme Activity
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Product Specifications
Source
E. coli-derived human Arginase 1/ARG1 protein
Met1-Lys322 with an N-terminal Met and 6-His tag
Met1-Lys322 with an N-terminal Met and 6-His tag
Purity
>90%, by SDS-PAGE under reducing conditions and visualized by silver stain.
Endotoxin Level
<1.0 EU per 1 μg of the protein by the LAL method.
N-terminal Sequence Analysis
Met
Predicted Molecular Mass
36 kDa
SDS-PAGE
40 kDa, reducing conditions
Activity
Measured by the production of urea during the hydrolysis of arginine.
The specific activity is >35,000 pmol/min/μg, as measured under the described conditions.
The specific activity is >35,000 pmol/min/μg, as measured under the described conditions.
Formulation, Preparation, and Storage
5868-AR
| Formulation | Supplied as a 0.2 μm filtered solution in Tris, NaCl, Glycerol and DTT. |
| Shipping | The product is shipped with dry ice or equivalent. Upon receipt, store it immediately at the temperature recommended below. |
| Stability & Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
|
Background: Arginase 1/ARG1
References
- Dowling, D. et al. (2008) Cell Mol. Life Sci. 65:2039.
- Durante, W. et al. (2007) Clin. Exp. Pharmacol. Physiol. 34:906.
- Morris, S. (2009) Br. J. Pharmacol. 157:922.
- Crombez, E. et al. (2005) Mol. Genet. Metab. 84:243.
- Scaglia, F. et al. (2004) J. Nutr. 134:2775s.
Long Name
Liver-Type Arginase
Alternate Names
AI, ARG1, Arginase-1, Liver Arginase, PGIF, Type I Arginase
Gene Symbol
ARG1
UniProt
Additional Arginase 1/ARG1 Products
Product Documents for Recombinant Human Arginase 1/ARG1 Protein, CF
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Recombinant Human Arginase 1/ARG1 Protein, CF
For research use only
Related Research Areas
Citations for Recombinant Human Arginase 1/ARG1 Protein, CF
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Protocols
View specific protocols for Recombinant Human Arginase 1/ARG1 Protein, CF (5868-AR):
Materials
- Assay Diluent: Deionized Water
- Recombinant Human Arginase 1/ARG1 (rhARG1) (Catalog # 5868-AR)
- Substrate Buffer: 125 mM L-Arginine, 625 mM Glycine, pH 10.5
- Manganese Choride, 1 M stock in deionized water
- o-Phthaldialdehyde (oPA), (Sigma, Catalog # P0657), 50 mg/mL (373 mM) stock in DMSO
- N-(1-Naphthyl)ethylene-diamine dihydrochloride (NED) (Sigma, Catalog # N9125), 500 mM stock in DMSO
- 50 mM Boric Acid, 1 M Sulfuric Acid, 0.03% Brij-35 (w/v) [Caution: highly acidic, neutralize before disposal]
- Urea, 100 mM stock in deionized water
- 96-well Clear Plate (Costar, Catalog # 92592)
- Plate Reader (Model: SpectraMax Plus by Molecular Devices) or equivalent
- Dilute rhARG1 to 0.25 µg/mL in deionized water.
- Prepare a standard curve from the 100 mM Urea stock. Dilute 100 µL of 100 mM Urea with 900 µL of deionized water to make a 10 mM Urea solution. Use this for the first point of the curve.
- Perform six additional one-half serial dilutions of the 10 mM Urea stock in deionized water. The standard curve has a range of 7813 to 500,000 pmol per well.
- Load 50 µL of each dilution of the standard curve into a plate. Include a blank containing only deionized water.
- Load 40 µL of the 0.25 µg/mL rhARG1 into the plate. Load multiple wells as some will be used as enzyme blanks.
- From the Substrate Buffer and Manganese Chloride stocks, prepare a solution of 100 mM Arginine, 500 mM Glycine, 1.25 mM MnCl2, pH 10.5. Do not prepare this solution until immediately before use as the manganese will gradually precipitate out of solution.
- Add 10 µL of 100 mM Arginine, 500 mM Glycine, 1.25 mM MnCl2, pH 10.5 to the wells containing 0.25 µg/mL rhARG1 (exclude the blanks). Mix well.
- Cover the plate and incubate at 37 °C for two hours.
- Dilute oPA stock to 4 mM in 50 mM Boric Acid, 1 M Sulfuric Acid, 0.03% Brij-35 (w/v).
- Dilute NED stock to 4 mM in 50 mM Boric Acid, 1 M Sulfuric Acid, 0.03% Brij-35 (w/v).
- Combine equal volumes of 4 mM oPA and 4 mM NED to form a solution of 2 mM oPA with 2 mM NED.
- Add 200 µL of the 2 mM oPA, 2 mM NED solution to all wells, including the standard curve.
- Prepare a fresh solution of 100 mM Arginine, 500 mM Glycine, 1.25 mM MnCl2, pH 10.5. Add 10 µL to each well used as an enzyme blank.
- Cover the plate and incubate at room temperature for 20 minutes.
- Read plate at 520 nm (absorbance) in endpoint mode.
- Calculate specific activity:
|
Specific Activity (pmol/min/µg) = |
Adjusted Urea Detected* (OD) |
| Incubation time (min) x amount of enzyme (µg) |
*Derived from the urea standard curve using linear or 4-parameter fitting and adjusted for Substrate Blank.
Per Well:- rhARG1: 0.01 µg (10 ng)
- Arginine: 4 mM
- oPA & NED: 1.6 mM
- Urea Curve: 500000, 250000, 125000, 62500, 31250, 15625 and 7813 pmol
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