| Literature DB >> 27699125 |
Pierre Mangeol1, Erwin J G Peterman2.
Abstract
Most methods to observe three-dimensional processes in living samples are based on imaging a single plane that is sequentially scanned through the sample. Sequential scanning is inherently slow, which can make it difficult to capture objects moving quickly in three dimensions. Here we present a novel method, multiple point-of-view microscopy (MPoVM), that allows simultaneous capturing of the front and side views of a sample with high resolution. MPoVM can be implemented in most fluorescence microscopes, offering new opportunities in the study of dynamic biological processes in three dimensions.Keywords: (170.6900) Three-dimensional microscopy; (180.2520) Fluorescence microscopy; (230.3990) Micro-optical devices
Year: 2016 PMID: 27699125 PMCID: PMC5030037 DOI: 10.1364/BOE.7.003631
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732