A conventional microscope produces a sharp image from just a single object-plane. This is often a limitation, notably in cell biology. We present a microscope attachment which records sharp images from several object-planes simultaneously. The key concept is to introduce a distorted diffraction grating into the optical system, establishing an order-dependent focussing power in order to generate several images, each arising from a different object-plane. We exploit this multiplane imaging not just for bio-imaging but also for nano-particle tracking, achieving similar to 10 nm z position resolution by parameterising the images with an image sharpness metric. (C)2010 Optical Society of America</p
Optical microscopy techniques such as single-particle tracking and high-resolution (<500 nm) imaging...
Optical microscopes allow us to study highly dynamic events from the molecular scale up to the whole...
We developed a new method for real-time, three-dimensional tracking of fluorescent particles. The in...
Observing biological processes in real-time and in single live cells is a vital step towards underst...
Due to the classical conflict between spatial and temporal resolution, microscopy studies of fast ev...
The distance separating two biomolecules in close proximity is an important determinant of the natur...
Recent technological advances have rendered widefield fluorescence microscopy as an invaluable tool ...
Conventional acquisition of three-dimensional (3D) microscopy data requires sequential z scanning an...
We describe the aberrations induced by introducing micromirrors into the object space of a microscop...
The imaging of cellular dynamics in three dimensions using a standard microscope is severely limited...
Using single molecule microscopy, biological interactions can be imaged and studied at the level of ...
The overwhelming effort in the development of new microscopy methods has been focused on increasing ...
The study of cellular processes in three-dimensions is severely limited by the lack of imaging metho...
Fluorescence microscopy provides an unparalleled tool for imaging biological samples. However, produ...
Multifocus microscopy (MFM) allows high-resolution instantaneous three-dimensional (3D) imaging and ...
Optical microscopy techniques such as single-particle tracking and high-resolution (<500 nm) imaging...
Optical microscopes allow us to study highly dynamic events from the molecular scale up to the whole...
We developed a new method for real-time, three-dimensional tracking of fluorescent particles. The in...
Observing biological processes in real-time and in single live cells is a vital step towards underst...
Due to the classical conflict between spatial and temporal resolution, microscopy studies of fast ev...
The distance separating two biomolecules in close proximity is an important determinant of the natur...
Recent technological advances have rendered widefield fluorescence microscopy as an invaluable tool ...
Conventional acquisition of three-dimensional (3D) microscopy data requires sequential z scanning an...
We describe the aberrations induced by introducing micromirrors into the object space of a microscop...
The imaging of cellular dynamics in three dimensions using a standard microscope is severely limited...
Using single molecule microscopy, biological interactions can be imaged and studied at the level of ...
The overwhelming effort in the development of new microscopy methods has been focused on increasing ...
The study of cellular processes in three-dimensions is severely limited by the lack of imaging metho...
Fluorescence microscopy provides an unparalleled tool for imaging biological samples. However, produ...
Multifocus microscopy (MFM) allows high-resolution instantaneous three-dimensional (3D) imaging and ...
Optical microscopy techniques such as single-particle tracking and high-resolution (<500 nm) imaging...
Optical microscopes allow us to study highly dynamic events from the molecular scale up to the whole...
We developed a new method for real-time, three-dimensional tracking of fluorescent particles. The in...