scholarly journals Isolation and Characterization of Bovine Plasminogen Activator from a Human Plasminogen-Streptokinase Mixture

1967 ◽  
Vol 242 (7) ◽  
pp. 1419-1425 ◽  
Author(s):  
Chung-Mei Ling ◽  
Louis Summaria ◽  
Kenneth C. Robbins
1974 ◽  
Vol 31 (01) ◽  
pp. 072-085 ◽  
Author(s):  
M Kopitar ◽  
M Stegnar ◽  
B Accetto ◽  
D Lebez

SummaryPlasminogen activator was isolated from disrupted pig leucocytes by the aid of DEAE chromatography, gel filtration on Sephadex G-100 and final purification on CM cellulose, or by preparative gel electrophoresis.Isolated plasminogen activator corresponds No. 3 band of the starting sample of leucocyte cells (that is composed from 10 gel electrophoretic bands).pH optimum was found to be in pH range 8.0–8.5 and the highest pH stability is between pH range 5.0–8.0.Inhibition studies of isolated plasminogen activator were performed with EACA, AMCHA, PAMBA and Trasylol, using Anson and Astrup method. By Astrup method 100% inhibition was found with EACA and Trasylol and 30% with AMCHA. PAMBA gave 60% inhibition already at concentration 10–3 M/ml. Molecular weight of plasminogen activator was determined by gel filtration on Sephadex G-100. The value obtained from 4 different samples was found to be 28000–30500.


1988 ◽  
Vol 2 ◽  
pp. 11
Author(s):  
M.R. Martzen ◽  
T.E. Petersen ◽  
A. Ichinose ◽  
E.W. Davie

Hepatology ◽  
1992 ◽  
Vol 16 (1) ◽  
pp. 54-59 ◽  
Author(s):  
Marlies Otter ◽  
PETRA Žočková ◽  
Johan Kuiper ◽  
Theo J. C. Van Berkel ◽  
Marrie M. Barrett-Bergshoeff ◽  
...  

1990 ◽  
Vol 265 (4) ◽  
pp. 2078-2085
Author(s):  
C J Bruzdzinski ◽  
M Riordan-Johnson ◽  
E C Nordby ◽  
S M Suter ◽  
T D Gelehrter

2020 ◽  
Vol 13 (6) ◽  
pp. 50-57
Author(s):  
T. A. Yatsenko ◽  

The plasminogen/plasmin system plays a crucial role in fibrinolysis and regulation of cell functions in a wide range of normal and pathological processes. Investigation of plasminogen/plasmin functions requires the availability of well-characterized and effective molecular tools, such as antibodies. In the present work, the isolation and characterization of rabbit polyclonal antibodies against human plasminogen are described and approaches for the identification of plasminogen and its fragments using the purified antibodies are demonstrated. For the antibodies isolation, standard animal immunization and blood collection procedures, serum isolation, protein salting out and affinity chromatography were performed. For the antibodies characterization and application, the following methods were used: enzyme linked immunoassay (ELISA), Western blotting, FITC-protein conjugation, flow cytometry and spectrofluorometry. The obtained polyclonal rabbit anti-human plasminogen antibodies interacted with human Glu- and Lys-plasminogen, kringles 1-3 and 1-4 of plasminogen, mini-plasminogen, the heavy and light chain of plasmin. We propose the application of anti-plasminogen antibodies for the direct ELISA, Western blot analysis, and for flow cytometry and spectrofluorometric analysis of plasminogen binding with cells. The obtained anti-plasminogen antibodies are promising tools for the investigation of plasminogen/plasmin system functions, either fibrinolytic or signaling.


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