Recombinant Mouse u-Plasminogen Activator (uPA) Protein, CF

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Recombinant Mouse u-Plasminogen Activator (uPA)/Urokinase His-tag (Catalog # 11143-SE) is measured by its ability to cleave a peptide substrate, N-carbobenzyloxy-Gly-Gly-Arg-7-amido-4-methylcoumarin (Z-GGR-AMC).

Product Details

Summary
Reactivity MuSpecies Glossary
Applications Enzyme Activity
Format
Carrier-Free

Order Details

Recombinant Mouse u-Plasminogen Activator (uPA) Protein, CF Summary

Additional Information
His-tag
Details of Functionality
Measured by its ability to cleave a peptide substrate, N-carbobenzyloxy-Gly-Gly-Arg-7-amido-4-methylcoumarin (Z-GGR-AMC). The specific activity is >1700 pmol/min/μg, as measured under the described conditions.
Source
Mouse myeloma cell line, NS0-derived mouse u-Plasminogen Activator (uPA)/Urokinase protein
Gly21-Phe433, with a C-terminal 6-His tag
Accession #
N-terminal Sequence
Lys157, Ile180, Met361
Protein/Peptide Type
Recombinant Enzymes
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Enzyme Activity
Theoretical MW
18 kDa (long A chain), 3 kDa (short A chain), 29 kDa (B chain).
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
24-33 kDa (short form), under non-reducing conditions
Publications
Read Publication using
11143-SE in the following applications:

Packaging, Storage & Formulations

Storage
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 opening.
Buffer
Supplied as a 0.2 μm filtered solution in HEPES, NaCl and CaCl2.
Purity
>90%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Assay Procedure
  • Assay Buffer: 50 mM Tris, 0.01% (v/v) Tween® 20, pH 8.5
  • Recombinant Mouse u-Plasminogen Activator (uPA)/Urokinase (rmuPA) (Catalog # 11143-SE)
  • Substrate: Z-Gly-Gly-Arg-AMC (Bachem, Catalog # I-1140), 10 mM stock in DMSO
  • F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
  • Fluorescent Plate Reader (Model: SpectraMax M5 by Molecular Devices) or equivalent
  1. Dilute rmuPA to 1 ng/µL in Assay Buffer.
  2. Dilute Substrate to 2 mM in Assay Buffer.
  3. Load 50 μL of 1 ng/µL rmuPA into a black well plate, and start the reaction by adding 50 µL of 2 mM Substrate. Include a Substrate Blank containing 50 µL of Assay buffer and 50 µL of 2 mM Substrate.
  4. Read at excitation and emission wavelengths of 380 nm and 460 nm (top read), respectively, in kinetic mode for 5 minutes.
  5. 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 from calibration standard 7-amino, 4-Methyl Coumarin (Sigma, Catalog # A9891)
Per Well:
  • rmuPA: 0.05 µg
  • Substrate: 1 mM

























Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Mouse u-Plasminogen Activator (uPA) Protein, CF

  • ATF
  • EC 3.4.21
  • EC 3.4.21.73
  • plasminogen activator, urokinase
  • PLAU
  • uPA
  • u-PA
  • uPlasminogen Activator
  • u-Plasminogen Activator
  • urinary
  • Urokinase
  • urokinase-type plasminogen activator

Background

Urokinase Plasminogen Activator (uPA), also known as u-plasminogen activator or urokinase, is a highly-specific serine protease from the peptidase S1 family that cleaves plasminogen to form plasmin making it a key player in the plasminogen activator (PA) system (1, 2). In cancer, the PA system plays a commanding role in tumor growth, angiogenesis, tumor cell invasion, migration, and metastasis. Expression of uPA is minimal in normal cells but is increased several fold in tumor cells by extracellular stimuli elevated in cancer (3) and corresponds to poor outcomes in several types of cancer (2, 4-7). Therefore, uPA has been identified as an excellent target for therapeutic development through inhibition of protease activity or though inhibition of uPA-dependent signaling while in complex with uPA receptor (uPAR) (2, 7). The pro-enzyme of uPA is synthesized with an N-terminal signal peptide and processed into an active disulfide-linked two-chain molecule (2, 7-10). For mouse uPA, the B chain starting at Ile180 corresponds to the catalytic domain. Two forms of the A chain exist, one starting at Gly21 (the long form) and the other at Lys157 (the short form). While the B chain is common for both forms, the long and short A chains are unique to expected 47 kDa and 32 kDa two-chain forms, respectively. The long A chain contains an EGF-like domain and the kringle domain. The long A domain is reported as responsible for the binding of the uPA receptor (uPAR) (2, 7).
  1. Ellis, V. (2004) in Handbook of Proteolytic Enzymes. Barrett, A.J. et al. eds., Academic Press, San Diego, pp.1677. 
  2. Mahmood, N. et al. (2018) Front Oncol. 8:24.
  3. Nagamine, Y. et al. (2005) Thromb. Haemost. 93:661.
  4. Duffy, M. and C. Duggan. (2004) Clin. Biochem. 37:541.
  5. Pappot, H. et al. (2006) Lung Cancer 51:193.
  6. Taubert, H. et al. (2010) Br. J. Cancer 102:731.
  7. Masucci, M.T. et al. (2022) Cancers. 14:498.
  8. Riccio, A. et al. (1985) Nucleic Acids Res. 13:2759.
  9. Nagai, M. et al. (1985) Gene 36:183.
  10. Jacobs, P. et al. (1985) DNA 4:139.

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Publications for u-Plasminogen Activator/Urokinase (11143-SE)(1)

We have publications tested in 1 confirmed species: Mouse.

We have publications tested in 1 application: Bioassay.


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