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About This Item
CAS Number:
UNSPSC Code:
12352202
NACRES:
NA.25
MDL number:
description
Merck USA index - 14, 7520
form
liquid
specific activity
≥5 units/mg protein
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
avoid repeated freeze/thaw cycles
shipped in
wet ice
storage temp.
−20°C
Quality Level
Preparation Note
Prepared from plasma that has been shown by certified tests to be negative for HBsAg and for antibodies to HIV and HCV.
Following initial thaw, aliquot and freeze (-20°C).
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
RESEARCH USE ONLY. This product is regulated in France when intended to be used for scientific purposes, including for import and export activities (Article L 1211-1 paragraph 2 of the Public Health Code). The purchaser (i.e. enduser) is required to obtain an import authorization from the France Ministry of Research referred in the Article L1245-5-1 II. of Public Health Code. By ordering this product, you are confirming that you have obtained the proper import authorization.
Toxicity: Standard Handling (A)
General description
Native plasmin from human plasma. Catalyzes the hydrolysis of peptides, arginine and lysine esters and converts fibrin into soluble products.
Other Notes
Federici, A.B., et al. 1993. Blood 81, 720.
Hoffmann, J.J., and Janssen, W.C. 1992. Thromb. Res. 67, 711.
Hoffmann, J.J., and Janssen, W.C. 1992. Thromb. Res. 67, 711.
One unit is defined as the amount of enzyme that will hydrolyze 1.0 µmol of N-tosyl-Gly-Pro-Lys-pNA per min at 25°C, pH 7.8.
Packaging
Please refer to vial label for lot-specific concentration.
Physical form
In 100 mM sodium phosphate, 1 mM 6-aminohexanoic acid, 25% glycerol, pH 7.3.
Storage Class
10 - Combustible liquids
wgk
WGK 2
Certificates of Analysis (COA)
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A B Federici et al.
Blood, 81(3), 720-725 (1993-02-01)
The behavior of plasma von Willebrand factor (vWF) in patients with acute leukemia (n = 5), decompensated cirrhosis (n = 10), and acute pancreatitis (n = 5) was investigated to evaluate whether the systemic proteolytic states associated with these diseases
J J Hoffmann et al.
Thrombosis research, 67(6), 711-719 (1992-09-15)
The mechanisms by which thrombolytic agents affect platelet function are not yet elucidated. The aim of the present study was to investigate the effects of plasmin, generated by thrombolytic agents in plasma, on platelet glycoproteins (GP) Ib and IIb/IIIa. Platelet-rich
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