| Literature DB >> 24733809 |
Thorsten Kolb1, Sahradha Albert, Michael Haug, Graeme Whyte.
Abstract
Flow cytometry provides a high throughput, multi-dimensional analysis of cells flowing in suspension. In order to combine this feature with the ability to resolve detailed structures in 3D, we developed an optofluidic device that combines a microfluidic system with a dual beam trap. This allows for the rotation of single cells in a continuous flow, around an axis perpendicular to the imaging plane. The combination of both techniques enables the tomographic reconstruction of the 3D structure of the cell. In addition this method is capable to provide detailed 3D structural data for flow cytometry, as it improves the reconstructed z-resolution of a standard microscopy system to produce images with isotropic resolution in all three axes.Entities:
Keywords: flow cytometry; optical trapping; single-cell analysis; tomography
Mesh:
Year: 2014 PMID: 24733809 DOI: 10.1002/jbio.201300196
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.207