[Development of a rapid method of immunoassay of C reactive protein by polarization of fluorescence]
Related Experiment Video
Updated: Sep 19, 2026

Rapid and Robust Analysis of Cellular and Molecular Polarization Induced by Chemokine Signaling
Published on: December 12, 2014
C Benattar1, J Francoual, J F Magny
1Laboratoire de Biochimie, Hôpital Antoine-Béclère, Clamart.
Abstract:
Increased level of C reactive protein in the serum of neonates indicates the presence of infection, whereas the classic signs (hyperthermia, neutrophilia...) may often fail. So the determination of C reactive protein is useful and has to be rapidly performed on a small quantity of blood. The authors evaluate a fluorescence-polarization immunoassay (TDX Abbott System), and compare this method to the radial immunodiffusion (RID) and the laser immunonephelemetry. Sensitivity (detection limit = 10 mg/l), reproducibility (cv less than 5 p. cent), linearity (until 243 mg/l), are satisfactory. The assay correlates well with RID (r = 0.98, p less than 0.001) and laser immunonephelometry (r = 0.93, p less than 0.001). The proposed method is rapid (10 minutes), requires small quantities of blood (less than 100 microliters), and is not influenced by important amounts of haemoglobin, bilirubin or triglycerides. Thus, this method provides a good means for C reactive protein determination, especially in neonates.
Related Concept Videos
Enzyme-Linked Immunosorbent Assay
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen. Enzyme-substrate reaction allows the antigen to be visualized or quantified.
Immunofluorescence Microscopy
The...

