The usefulness of paper discs in the immunoprecipitation reaction in agar gel

Life Sciences ◽  
1966 ◽  
Vol 5 (17) ◽  
pp. 1605-1610 ◽  
Author(s):  
RenéJ. Duquesnoy
1998 ◽  
Vol 2 (1) ◽  
pp. 67-70
Author(s):  
Akihiro C. Yamashita ◽  
Ryoichi Sakiyama ◽  
Hiroyuki Hamada ◽  
Kakuji J. Tojo

1974 ◽  
Vol 32 (02/03) ◽  
pp. 356-365 ◽  
Author(s):  
F Haverkate ◽  
D. W Traas

SummaryIn the fibrin plate assay different types of relationships between the dose of applied proteolytic enzyme and the response have been previously reported. This study was undertaken to determine whether a generally valid relationship might exist.Trypsin, chymotrypsin, papain, the plasminogen activator urokinase and all of the microbial proteases investigated, including brinase gave a linear relationship between the logarithm of the enzyme concentration and the diameter of the circular lysed zone. A similar linearity of dose-response curves has frequently been found by investigators who used enzyme plate assays with substrates different from fibrin incorporated in an agar gel. Consequently, it seems that this linearity of dose-response curves is generally valid for the fibrin plate assay as well as for other enzyme plate bioassays.Both human plasmin and porcine tissue activator of plasminogen showed deviations from linearity of semi-logarithmic dose-response curves in the fibrin plate assay.


1981 ◽  
Vol 19 (2) ◽  
pp. 101 ◽  
Author(s):  
Won Young Choi ◽  
Ok Ran Lee
Keyword(s):  

1979 ◽  
Author(s):  
E.J. McKay

Depressed Antithrombin III (AT) levels Increase thrombic tendency in man, therefore value in assaying this protein has been established. Immunochemical analysis of AT in clinical disease has however proved controversial, consequently systematic studies were undertaken to rationalize the requirements necessary to optimise these methods in particular electro-Immunoassay. The known binding affinity of AT for heparin has been exploited to differentiate high affinity AT from its inhibitor - protease complexes and has resulted in reports stating that heparin added to the agar gel prior to electrophoresis significantly reduces the time required for completion of antigen/antibody complexes. Our studies however have demonstrated that the antibody required for quantitative analysis must be capable of not only reacting with “native” antigenic determinants of AT but also with “neo” antigens that are exposed when inhibitor-protease complexes are formed. Heparin should not be used in the test protocol, for it has a paradoxical effect on Immunopreclpltation in gels, masking some antigenic determinants of unbound - high affinity AT on one hand, and appear to disrupt the Immunoprecipitin “rocket” formed with the inhibitor-protease complexes during electrophoresis on the other.


2008 ◽  
Vol 109 (4) ◽  
pp. 703-708 ◽  
Author(s):  
Tuoping Li ◽  
Suhong Li ◽  
Na Wang ◽  
Lirui Tain
Keyword(s):  

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