Ultra-fast simultaneous detection of obesity-related coenzymes in mice using microchip electrophoresis with a LIF detector

2008 ◽  
Vol 619 (1) ◽  
pp. 94-100 ◽  
Author(s):  
Hee Gu Lee ◽  
K.S. Kumar ◽  
Ju-Ryoun Soh ◽  
Youn-Soo Cha ◽  
Seong Ho Kang
2006 ◽  
Vol 29 (7) ◽  
pp. 1487-1489 ◽  
Author(s):  
Mohammad Jabasini ◽  
Ashraf Abdulazim Ewis ◽  
Maged Fouad ◽  
Fuquan Dang ◽  
Guichen Ping ◽  
...  

2017 ◽  
Vol 9 (48) ◽  
pp. 6785-6790 ◽  
Author(s):  
Jian Li ◽  
Jingjin Zhao ◽  
Shuting Li ◽  
Liangliang Zhang ◽  
Chuanqing Lan ◽  
...  

A G-quadruplex DNAzyme and nicking enzyme assisted multiplex chemiluminescence signal amplification based microchip electrophoresis method was developed for simultaneous detection of two trace biomolecules.


1996 ◽  
Vol 76 (06) ◽  
pp. 1090-1095 ◽  
Author(s):  
C Ravanat ◽  
M Freund ◽  
S Schuhler ◽  
P Grunert ◽  
L Meyer ◽  
...  

SummaryThe purpose of this study was to develop specific and sensitive immunoassays to detect early indices of hypercoagulability in the rat. Rat platelet factor 4 (rPF4) and rat fibrinopeptide A (rFPA) assays, tools for the detection of activation of platelets and coagulation respectively, were designed using antibodies raised against purified rPF4 and against synthetic rFPA. The relevance of these new assays and of the commercially available ELISA kit for thrombin-antithrombin III (TAT) complexes was demonstrated in a rat model of a prethrombotic state induced by intravenous infusion of varying doses of thromboplastin (90 to 2400 μl/kg/h). In this model, the immunoassays allowed simultaneous detection of low levels of rFPA and rPF4 which were correlated with fibrinogen and platelet consumption and TAT generation and further proved to be of higher sensitivity than the classical methods of platelet count or measurement of fibrinogen levels. Plasma concentrations of rFPA, rPF4 and TAT were dependent on infusion time and thromboplastin dose, while hirudin (1 mg/kg) prevented their appearance. Thus the new specific immunoassays for rPF4 and rFPA and the commercial human TAT assay represent useful tools for pathophysiological studies or the screening of antithrombotic drugs in rats.


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