Evaluation of 2-Methacryloyloxyethyl Phosphorylcholine Polymeric Nanoparticle for Immunoassay of C-Reactive Protein Detection

2004 ◽  
Vol 76 (9) ◽  
pp. 2649-2655 ◽  
Author(s):  
Jongwon Park ◽  
Shigeru Kurosawa ◽  
Junji Watanabe ◽  
Kazuhiko Ishihara
Keyword(s):  
Protein Detection ◽  
C Reactive Protein ◽  
Reactive Protein ◽  
Polymeric Nanoparticle

Myocardial Infarction Biomarker C‐reactive Protein Detection on Nanocomposite Aptasensor

2020 ◽  
Author(s):  
Jing Li ◽  
Haitao Li ◽  
Jinpeng Xu ◽  
Xingzhou Zhao ◽  
Shujiang Song ◽  
...  
Keyword(s):  
Myocardial Infarction ◽  
Protein Detection ◽  
C Reactive Protein ◽  
Reactive Protein

scholarly journals Surface Plasmon Resonance for C-Reactive Protein Detection in Human Plasma

2014 ◽  
Vol 05 (03) ◽  
pp. 153-158 ◽  
Author(s):  
Hanen Chammem ◽  
Imen Hafaid ◽  
Olivier Meilhac ◽  
Farid Menaa ◽  
Laurence Mora ◽  
...  
Keyword(s):  
Surface Plasmon Resonance ◽  
Human Plasma ◽  
Surface Plasmon ◽  
Plasmon Resonance ◽  
Protein Detection ◽  
C Reactive Protein ◽  
Reactive Protein

Disposable Polydimethylsiloxane/Silicon Hybrid Chips for Protein Detection

2004 ◽  
Author(s):  
Shifeng Li ◽  
David Fozdar ◽  
Dongbing Shao ◽  
Shaochen Chen ◽  
Pierre N. Floriano ◽  
...  
Keyword(s):  
Protein Detection ◽  
Ccd Camera ◽  
Multiplex Assay ◽  
Pdms Layer ◽  
C Reactive Protein ◽  
Fluorescent Assay ◽  
Reactive Protein ◽  
Agarose Beads ◽  
Fluid Network ◽  
Pressure Compensation

This paper presents disposable protein analysis chips with single and multiple chambers - constructed from poly (dimethylsiloxane) (PDMS) and silicon. The chips are composed of a multilayer stack of PDMS layers that sandwich a silicon microchip. This inner silicon chip features an etched array of microcavities hosting agarose beads. The sample is introduced into the fluid network in the top PDMS layer where it is directed to the bead chamber. After reaction of the analyte with the probe beads, signal generated on the beads is captured with a CCD camera, digitally processed, and analyzed. An established bead-based fluorescent assay for C-reactive protein (CRP) was used here to characterize these hybrid chips. The detection limit of the single chamber protein chip was found to be 1ng/mL. Additionally, using the back pressure compensation method, the signals from each of the four-chamber chip were found to be within 10% of each other. Moreover, the fabrication of the multiple-chamber chip may increase throughput and multiplex assay capacity.

A simple label-free aptamer-based method for C-reactive protein detection

2016 ◽  
Vol 8 (21) ◽  
pp. 4177-4180 ◽  
Author(s):  
Bin Wu ◽  
Nandi Chen ◽  
Qing Wang ◽  
Xiaohai Yang ◽  
Kemin Wang ◽  
...  
Keyword(s):  
Protein Detection ◽  
Label Free ◽  
C Reactive Protein ◽  
Reactive Protein

We developed a simple label-free aptamer-based method for C-reactive protein (CRP) detection.

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