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Dive into the research topics where G.A.J. Besselink is active.

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Featured researches published by G.A.J. Besselink.


Biosensors and Bioelectronics | 2003

Modification of ISFETs with a monolayer of latex beads for specific detection of proteins

G.A.J. Besselink; Richardus B.M. Schasfoort; Piet Bergveld

The so-called ion-step method is a novel potentiometric approach that can detect protein adsorbed onto the gate area of modified ion-sensitive field-effect transistors (ISFETs). In this report, a generic technology is described for immobilization of peptides and proteins to the ISFET gate in order to confer specific binding properties to the ISFET. For this, the surface of the ISFET was covered with a monolayer of Amino beads (diameter, 0.9 microm) followed by immobilization of protein ligands onto these beads. Amino beads are latex spheres that contain primary amino groups at the outer surface. Preactivation of the latex-bound amino groups with glutaraldehyde, and consecutive incubation with polylysine resulted in covalent immobilization of this polyamine, as revealed by ion stepping measurements. For ImmunoFET applications, human serum albumin (HSA) was immobilized onto the Amino bead-covered ISFETs, by passive adsorption but also by covalent coupling. Resulting devices were used for qualitative detection of alpha-HSA antibodies by means of the ion step method. The binding of antibody was very specific and fast (most of the binding was accomplished in 15 min) with signal yields up to 17 mV. Efforts to increase the antibody-binding capacity of the solid phase on the ISFET exploiting amino group activation (with glutaraldehyde or other homobifunctional cross linkers) before HSA coupling, did not improve signal yield. The bead technology described in this report is an easy, generic method for coating the ISFET with a solid phase that, using the ion-step method, can be applied to immunosensing.


Biosensors and Bioelectronics | 2008

Angle-scanning SPR imaging for detection of biomolecular interactions on microarrays.

J.B. Beusink; A.M.C. Lokate; G.A.J. Besselink; Ger J. M. Pruijn; Richardus B.M. Schasfoort


Archive | 2006

SPR imaging for protein microarrays for detection of antibody binding

J.B. Beusink; G.A.J. Besselink; Richardus B.M. Schasfoort


Archive | 2005

A novel PDMS based approach for the fabrication of protein microarrays

J.B. Beusink; G.A.J. Besselink; Stefan Schlautmann; A.J. Tudos; Richardus B.M. Schasfoort


8th International Conference on Micro Total Analysis Systems, µTAS 2004 | 2004

Proteomics in microfabricated devices

Richardus B.M. Schasfoort; Stefan Schlautmann; G.A.J. Besselink; A.J. Tudos; T Laurell; J Nilsson; K Jensen; D.J. Harrison; J.P. Kutter


Archive | 2006

Automated SPR imaging of peptide microarrays for analyte detection for multi-analyte detection of Rheumatoid Arthritis

A.C.M. Lokate; J.B. Beusink; G.A.J. Besselink; Ger J. M. Pruijn; Richardus B.M. Schasfoort


Archive | 2005

Microfabricated free-flow electrophoresis device with integrated salt bridge structures

D. Kohlheyer; Stefan Schlautmann; G.A.J. Besselink; Richardus B.M. Schasfoort


Archive | 2005

Free-Flow-Electrophoresis chip with microfabricated salt-bridges

D. Kohlheyer; G.A.J. Besselink; Stefan Schlautmann; Richardus B.M. Schasfoort


Archive | 2005

Techniques for creating microarrays for surface plasmon resonance-based protein assay

R. Verdoold; M.B.M. Harink; J.B. Beusink; G.A.J. Besselink; Richardus B.M. Schasfoort


9th International Conference on Miniaturized Systems for Chemistry and Life Sciences, µTAS 2005 | 2005

Imaging Surface Plasmon Resonance for Monitoring Biomolecular Interactions in Microfluidic Devices

Richardus B.M. Schasfoort; J.B. Beusink; Stefan Schlautmann; G.A.J. Besselink; A.J. Tudos; Gerard H.M. Engbers

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Wouter Olthuis

MESA+ Institute for Nanotechnology

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A.J. Tudos

MESA+ Institute for Nanotechnology

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Rob G.H. Lammertink

MESA+ Institute for Nanotechnology

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S. Bohm

University of Twente

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Ger J. M. Pruijn

Radboud University Nijmegen

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A.M.C. Lokate

Radboud University Nijmegen

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