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Urokinase, human

Catalog No. Size Price Figures
Z00054-100 ug
100 ug
$ 80.00

EXAMPLE:
Urokinase, human
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References:
  • Shetty S, Idell S. Post-transcriptional regulation of urokinase mRNA. Identification of a novel urokinase mRNA-binding protein in human lung epithelial cells in vitro. J Biol Chem. May 2000; 275(18): 13771-13779.
  • Hudson MA, McReynolds LM. Urokinase and the urokinase receptor: association with in vitro invasiveness of human bladder cancer cell lines. J Natl Cancer Inst. May 1997;89(10):709-717.
  • Nienaber V, et al. Re-engineering of human urokinase provides a system for structure-based drug design at high resolution and reveals a novel structural subsite. J Biol Chem. Mar 2000; 275(10): 7239-7248.
Full Name
Urokinase, human
Abbreviated Name-1Urokinase
DescriptionUrokinase (UK) is a serine protease, which is one of biological plasminogen activators. It is involved in a number of biological functions including fibrinolysis, embryogenesis, cell migration, tissue remodeling, ovulation, and wound healing. It can be obtained from human urine or kidney cell culture. UK is a two-chain glycoprotein containing 411 amino acids with 12 dissulfide bonds. Its molecular weight is 54,000 Da.
SourceHuman urine
M.W.54,000 Da
PurityGreater than 90.0% as determined by SDS-PAGE
Specific Activity1 nM UK will cause a change in absorbance of 0.001 at 405 nm in 1 minute at R/T in 100 ul 0.05 M Tris-HCl, 0.1 M NaCl, pH 7.4, using S2444 (0.6 mM) as the substrate. The hUK conforms an activity greater than 68,000 IU/mg.
StorageLyophilized hUK although stable at room temperature for 3 weeks, should be stored desiccated below -18°C. Upon reconstitution hUK should be stored at 4°C between 2-7 days and for future use below -18°C. Please prevent freeze-thaw cycles.
FormulationThe hUK was lyophilized from a concentrated (1 mg/ml) solution with no additives.
ReconstitutionIt is recommended to reconstitute the lyophilized hUK in sterile 18 MΩ-cm H2O not less than 100 µg/ml, which can then be further diluted to other aqueous solutions.
ConcentrationProtein quantitation was carried out by two independent methods:
1. UV spectroscopy at 280 nm.
2. Analysis by RP-HPLC, using a calibrated solution of hUK as a Reference Standard.
Quality ControlHepatitis B surface antigen, Hepatitis C antibody and HIV I and II
* For Non-Clinical Research Use Only *