Applied Precision, Inc.

Ge Healthcare Bio-sciences Corp.

Leica Microsystems Cms Gmbh

Steven A Reese

Paul Carlyle Goodwin

Carl S Brown

William Michael Dougherty

Jeremy R Cooper

David A Stewart

David Edward Stewart

James T Newberry

Kathryn Buckanan

Jeffrey D Bert

David Stewart

Disclosed is a cell culture microscopy slide comprising an optically transparent generally flat supporting surface () including upper and lower opposed substrate surfaces (). A peripheral frame () surrounds the substrate (), the frame () having a lower frame surface () and an upper frame surface (). The lower frame surface () and the lower substrate surface () are generally flush. The upper frame surface () lies above the upper substrate surface (), to form a well (), and the upper and lower frame surfaces () are continuously flat and generally parallel. The substrate is preferably glass having a thickness of 1.7 mm.

Cell culture microscopy slides

Methods and apparatus are described for delivering index-matching immersion liquid in high numerical-aperture optical microscopy and lithography. An array of immersion liquid droplets is delivered to a specimen substrate or specimen substrate cover by an immersion liquid printing apparatus. An immersion liquid reservoir provides immersion liquid to the printer by a precision pump. The printer delivers immersion liquid to the substrate or substrate cover in arrays of immersion liquid droplets of defined volumes and array patterns. The volumes and patterns of array droplets delivered to the substrate or substrate cover are optimized to maintain adequate immersion liquid between the substrate or substrate cover and an immersion objective while avoiding the formation of air bubbles in the immersion liquid and the accumulation of excess volumes of immersion liquid.

Dispersing immersion liquid for high resolution imaging and lithography

Illumination system for a microscope system capable of being mode-switchable between a first and a second illumination mode, comprising one source of light for providing a collimated beam of light, at least one selector mirror capable of being positioned in at least two positions to redirect the beam of light in two different beam paths, the first beam path being a direct exit beam path wherein the selector mirror redirects the beam of light along an exit beam path to provide a first illumination mode, the second beam path is a mirror loop path comprising two or more mirrors arranged to redirect the beam of light onto the selector mirror such that it is redirected by the selector mirror a second time along the exit beam path, and wherein mirror loop path comprises at least one optical element arranged to optically alter the beam of light to provide the second illumination mode. According to one embodiment, the first illumination mode is Total Internal Reflection (TIRF) and the second illumination mode is Photokinetics (PK) illumination.

Mode-switchable illumination system for a microscope

Irradiance control systems ('ICSs') that control the irradiance of a beam of light are disclosed. ICSs include in a beam translator and a beam launch. The beam translator translates the beam substantially perpendicular to the propagating direction of the beam with a desired displacement so that the beam launch can remove a portion of the translated beam and the beam can be output with a desired irradiance. The beam launch attenuates the irradiance of the beam based on the amount by which the beam is translated. ISCs can be incorporated into fluorescent microscopy instruments to provide high-speed, fine-tune control over the irradiance of excitation beams.

Laser beam irradiance control systems

A new optical substrate design allows a target to be illuminated with minimal illumination of undesired surfaces within the image collection ray path. The non rectangular substrate provide different surfaces through which a target is illuminated and imaged and thereby prevents illumination rays from crossing the substrate surface through which the target is imaged

Optical substrate for reduced background fluorescence

A system and method employing photokinetic techniques in cell biology imaging applications are disclosed. Systems and methods of acquiring image data of an object may comprise: selectively inducing photoactivation of material at a site on the object; performing an optical axis integration scan; simultaneously executing a time delay integration scan sequence; and processing acquired image data in accordance with one or more desired analyses. Various methodologies and applications may include, inter alia, selective photobleaching of a site on the object, diffusion rate, velocity, and wave-front propagation analyses, multi-dimensional analyses of dispersion characteristics, biomolecular binding in cellular organelles, and photoactivation assisted systematic image segmentation for the study of cellular components.

System and method employing photokinetic techniques in cell biology imaging applications

An image acquisition system and method employing multi-axis integration (MAI) may incorporate both optical axis integration (OAI) and time-delay integration (TDI) techniques. Disclosed MAI systems and methods may integrate image data in the z direction as the data are acquired, projecting the image data prior to deconvolution. Lateral translation of the image plane during the scan in the z direction may allow large areas to be imaged in a single scan sequence.

Growing community of inventors

Shoreline, WA, United States of America

Steven A Reese