CC4000
Urokinase-type Plasminogen Activator
Synonym(s):
uPA
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About This Item
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biological source
human
Quality Level
assay
>98% (SDS-PAGE)
form
solid
manufacturer/tradename
ChemiconĀ®
technique(s)
activity assay: suitable
NCBI accession no.
UniProt accession no.
shipped in
dry ice
Gene Information
human ... PLAU(5328)
General description
A thrombolytic agent that converts plasminogen to plasmin. A mixture of high molecular weight and low molecular weight urokinase.
Product Source: Prepared from urine of healthy individuals
Physical form
Lyophilized from 200 mM manitol, 100 mM NaCl, 50 mM Tris-HCl, pH 7.5 and 0.1 % PEG.
Storage and Stability
Reconstitute using 200-400 Ī¼L dH2O. Store at -20Ā°C. Following reconstitution, aliquot and freeze (-70Ā°C). This product is stable for 2 year as supplied. Stock solutions are stable for up to 6 months at -70Ā°C.
Analysis Note
High molecular weight urokinase (54 kD): 40%.Low molecular weight urokinase (33 kD): 50%.Transitory forms of urokinase: 10%
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
signalword
Danger
hcodes
pcodes
Hazard Classifications
Resp. Sens. 1
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
Certificates of Analysis (COA)
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Thrombolytic therapy: a comparison between urokinase and streptokinase. From a national cooperative study.
Seminars in thrombosis and hemostasis, 2(1), 1-13 (1975-07-01)
Assay methods and standard preparations for plasmin, plasminogen and urokinase in purified systems, 1967-1968.
Thrombosis et Diathesis Haemorrhagica, 21, 259-272 (1969)
Biomaterials, 30(23-24), 3825-3833 (2009-05-16)
Mass spectrometry is a powerful proteomic tool enabling researchers to survey the global proteome of a cell. This technique has only recently been employed to investigate cell-material interactions. We had previously identified material scarcity and limited adherent cells as challenges
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