A new method for the determination of peak distribution across a two-dimensional separation space for the identification of optimal column combinations

2016 ◽  
Vol 408 (28) ◽  
pp. 8079-8088 ◽  
Author(s):  
Juri Leonhardt ◽  
Thorsten Teutenberg ◽  
Greta Buschmann ◽  
Oliver Gassner ◽  
Torsten C. Schmidt
2001 ◽  
Vol 40 (Part 1, No. 1) ◽  
pp. 388-392
Author(s):  
Hiroyuki Fujishiro ◽  
Tatsuya Okamoto ◽  
Manabu Ikebe ◽  
Koichi Hirose

1975 ◽  
Vol 30 (5-6) ◽  
pp. 358-372 ◽  
Author(s):  
Rüdiger Blume ◽  
Jürgen Polster

The spectrophotometric titration of three-step sequential dissociation equilibria is analyzed by means of two dimensional absorbance diagrams. The evaluation of pK1 and pK3 as well as of the absorbance coefficients of both ampholytes is made by the uniform segments at the beginning and end of the titration. New methods of evaluating the value of pK2 precisely and without difficulty even at small pK-differences are described. By means of several independent criteria the pK-values and the absorbance coefficients of the ampholytes can be examined. The titration of (1,2,4)-benzenetricarboxylic acid illustrates the new method.


1960 ◽  
Vol 23 ◽  
pp. 227-232 ◽  
Author(s):  
P WEST ◽  
G LYLES
Keyword(s):  

1977 ◽  
Vol 37 (02) ◽  
pp. 210-215 ◽  
Author(s):  
R Margalit ◽  
E Gidron ◽  
Y Shalitin

SummaryThe term “effective activator” of plasminogen is proposed, to denote the resultant of activator-antiactivator interaction, and a method for the determination of the level of these activators is described. By adding axcess plasminogen to the euglobulin fraction of plasma the influence of the level of endogenous plasminogen and of the antiplasmin is eliminated. It is shown that the level of fibrinogen has very little bearing on the results. An effective activator unit is defined as equal to 1 CTA unit of urokinase activity on a fibrinogen-plasminogen substrate.


1964 ◽  
Vol 12 (01) ◽  
pp. 119-125 ◽  
Author(s):  
Y Shamash ◽  
A Rimon

SummaryA new method for the assay of plasmin inhibitors in human plasma is described. The method consists of determination of the caseinolytic activity of a standard plasmin solution before and after incubation with the inhibitor, with lysine added to the mixture as a stabilizer of plasmin. Using this method, it was found that plasma contains enough inhibitors to inactivate 30 caseinolytic units of plasmin, or 10 times the normal amount of plasminogen in human plasma.


1969 ◽  
Vol 62 (1_Suppl) ◽  
pp. S95-S112 ◽  
Author(s):  
A. H. W. M. Schuurs

ABSTRACT Various techniques for sensitising erythrocytes and latex particles with gonadotrophins, particularly with HCG, are described. The haemagglutination inhibition reactions are generally interpreted by means of »erythrocyte settling patterns«. By a new method of evaluating these patterns a relatively precise quantitative determination is possible. Latex agglutination inhibition reactions on slides are particularly suitable as rapid qualitative tests. In cases where the maximum attainable sensitivity of the agglutination inhibition tests is insufficient, e. g. for determining LH concentrations in urine, the hormone in the test fluid has to be concentrated or extracted. An alternative method is a modified haemagglutination inhibition test for large volumes which is applicable to unconcentrated urine. Due to non-specific inhibitions the above-mentioned tests cannot be applied to unprocessed serum. Agglutination inhibition tests with HCG are already well advanced, pregnancy diagnosis being their main application. Now that highly purified HCG is available, a satisfactory specificity for these tests can be attained. If the immune system for HCG is used for estimating LH, it has to meet additional specificity requirements. Furthermore, the measure of cross-reaction and the choice of standard merit special attention. Finally, a literature survey is given of test systems in which LH and FSH were used as antigens.


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