Measured by its ability to inhibit papain cleavage of a fluorogenic peptide substrate Z-FR-AMC (Catalog # ES009). The IC50 value is <10 nM, under the described conditions.
Source
Mouse myeloma cell line, NS0-derived mouse Cystatin C protein Met1-Ala140, with a C-terminal 10-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
Inhibition Activity
Theoretical MW
15 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.
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
6 months from date of receipt, -20 to -70 °C as supplied.
3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in HEPES and NaCl.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 100 μg/mL in sterile 25 mM HEPES and 150 mM NaCl, pH 7.8.
Assay Procedure
Activation Buffer: 50 mM Tris, 5 mM DTT, pH 7.0
Assay Buffer: 50 mM Tris, pH 7.0
Recombinant Mouse Cystatin C (rmCystatin C) (Catalog # 1238-PI)
Papain (Sigma, Catalog # P4762)
Substrate: Z-Phe-Arg-AMC (Catalog # ES009) , 10 mM stock in DMSO
F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
Chill Activation Buffer on ice.
Dilute Papain to 100 µg/mL in Activation Buffer.
Incubate at room temperature for 15 minutes to activate.
Prepare a dilution curve of rmCystatin C (MW: 14,768 Da) in Assay Buffer. Make the following serial dilutions: 3000 nM, 500 nM, 250 nM, 125 nM, 83.3 nM, 55.6 nM, 37.1 nM, 24.7 nM, and 8.23 nM.
Dilute activated Papain to 2 µg/mL in Assay Buffer.
Mix equal volumes of the rmCystatin C curve dilutions and the diluted active Papain. Include a control (in duplicate) containing Assay Buffer and the diluted active Papain.
Incubate mixtures at 37 °C for 15 minutes.
Dilute Substrate to 200 µM in Assay Buffer.
Perform a five-fold dilution with Assay Buffer to the incubated mixture of rmCystatin C and Papain.
Load 50 µL of diluted incubated mixture into a black well plate, and start the reaction by adding 50 µL of 200 µM Substrate.
Read at excitation and emission wavelengths of 380 nm and 460 nm, respectively, for 5 minutes in kinetic mode.
Derive the 50% inhibiting concentration (IC50) of rmCystatin C by plotting RFU/min (or specific activity) vs. concentration with 4-PL fitting.
The specific activity for Papain at each point may be determined using the following formula (if needed):
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 7-Amino, 4-Methyl Coumarin (AMC) (Sigma, Catalog # A-9891).
Per Well:
Papain: 0.01 µg
Substrate: 100 µM
rmCystatin C curve: 150, 25, 12.5, 6.25, 4.165, 2.78, 1.885, 1.235, and 0.412 nM
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse Cystatin C Protein, CF
ARMD11
bA218C14.4 (cystatin C)
CST3
cystatin 3
cystatin C (amyloid angiopathy and cerebral hemorrhage)
Cystatin C
cystatin-3
cystatin-C
Gamma-trace
MGC117328
Neuroendocrine basic polypeptide
Post-gamma-globulin
Background
Cystatin C is a member of family 2 of the cystatin superfamily (1). It is involved in processes such as tumor invasion and metastasis, inflammation and some neurological diseases. It inhibits many cysteine proteases such as papain and cathepsins B, H, K, L and S (2, 3). All mouse tissues analyzed expressed Cystatin C, with relative levels similar to those of rat and human tissues. For all three species, brain and liver had the highest and lowest levels of Cystatin C, respectively, whereas kidney, spleen and muscle had the levels in between (4). The high degree of similarity in distribution and functional properties for mouse, rat and human Cystatin C indicates that a murine model should be relevant for studies of the human disease, hereditary Cystatin C amyloid angiopathy (4).
Reed, C.H. (2000) British J. Biomed. Sci. 57:323.
Janowski, R. et al. (2001) Nat. Struct. Biol. 8:316.
Abrahamson, M. (1994) Methods Enzymol. 244:685.
Hakansson, K. et al. (1996) Comp. Biochem. Physiol. 114B:303.
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