Postdoctoral., Stanford University (USA); ; PhD, Swiss Federel Institute of Technology at Lausanne (EPFL, Switzerland); Dipl. Phys., University of Heidelberg, Germany.
Contact Information:
Office: S1A-02-12
Tel: (65)-6516-1248
Fax: (65)-6776-7882
Email: twohland@nus.edu.sg
My group works on the development of new fluorescence spectroscopy techniques for the measurement of biomolecular interactions in cells, tissues, and organisms. Specific foci are:
In recent years our group focused on developing image based fluorescence tech-niques in which the signal at each pixel of a camera is evaluated to determine sample structure, dynamics, and interactions and single molecule sensitivity. We have implemented these techniques on total internal reflection (TIR) and single plane illumination microscopes (SPIM). Abbreviations: FCS – fluorescence correlation spectroscopy; FCCS – fluorescence cross-correlation spectroscopy; N&B – number and brightness analysis; FRAP – Fluorescence Recovery After Photobleaching; SRRF – super-resolution radial fluctuation; SPT – single particle tracking; spFRET – single particle Förster resonance energy transfer.