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A highly versatile microscope imaging technology platform for the multiplex real-time detection of biomolecules and autoimmune antibodies.

Authors :
Rödiger S
Schierack P
Böhm A
Nitschke J
Berger I
Frömmel U
Schmidt C
Ruhland M
Schimke I
Roggenbuck D
Lehmann W
Schröder C
Source :
Advances in biochemical engineering/biotechnology [Adv Biochem Eng Biotechnol] 2013; Vol. 133, pp. 35-74.
Publication Year :
2013

Abstract

The analysis of different biomolecules is of prime importance for life science research and medical diagnostics. Due to the discovery of new molecules and new emerging bioanalytical problems, there is an ongoing demand for a technology platform that provides a broad range of assays with a user-friendly flexibility and rapid adaptability to new applications. Here we describe a highly versatile microscopy platform, VideoScan, for the rapid and simultaneous analysis of various assay formats based on fluorescence microscopic detection. The technological design is equally suitable for assays in solution, microbead-based assays and cell pattern recognition. The multiplex real-time capability for tracking of changes under dynamic heating conditions makes it a useful tool for PCR applications and nucleic acid hybridization, enabling kinetic data acquisition impossible to obtain by other technologies using endpoint detection. The paper discusses the technological principle of the platform regarding data acquisition and processing. Microbead-based and solution applications for the detection of diverse biomolecules, including antigens, antibodies, peptides, oligonucleotides and amplicons in small reaction volumes, are presented together with a high-content detection of autoimmune antibodies using a HEp-2 cell assay. Its adaptiveness and versatility gives VideoScan a competitive edge over other bioanalytical technologies.

Details

Language :
English
ISSN :
0724-6145
Volume :
133
Database :
MEDLINE
Journal :
Advances in biochemical engineering/biotechnology
Publication Type :
Academic Journal
Accession number :
22437246
Full Text :
https://doi.org/10.1007/10_2011_132