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The determination of cystatin C in biological samples via the surface plasmon resonance method
M. Lesnak, D. Jursa, M. Miskay, H. Riedlova, K. Barcova, M. Adamek
Language English Country Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Directory of Open Access Journals
from 2018
Freely Accessible Science Journals
from 1996
Taylor & Francis Open Access
from 1996-01-01
ROAD: Directory of Open Access Scholarly Resources
from 1983
PubMed
33998838
DOI
10.2144/btn-2020-0151
Knihovny.cz E-resources
- MeSH
- Biosensing Techniques * MeSH
- Cystatin C analysis urine MeSH
- Humans MeSH
- Microarray Analysis MeSH
- Mice MeSH
- Surface Plasmon Resonance * MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Surface plasmon resonance imaging biosensors have a number of advantages that make them superior to other analytical methods. These include the possibility of label-free detection, speed and high sensitivity to low protein concentrations. The aim of this study was to create and analyze biochips, with the help of which it is possible to test cystatin C in patient urine samples and compare the results with the one-time traditional ELISA method. The main advantage of the surface plasmon resonance imaging method is the possibility of repeated measurements over a long period of time in accordance with clinical practice. The surface of the biochip was spotted with anticystatin C and a negative control of mouse IgG at a ratio of 1:1. The aforementioned biochip was first verified using standard tests and then with patient samples, which clearly confirmed the required sensitivity even for very low concentrations of cystatin C.
References provided by Crossref.org
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