Molecular Devices Corporation

Molecular Devices (austria) Gmbh

Georg Kronberger

Michael Katzlinger

Bernhard Schinwald

Josef J Atzler

Daniel M Stock

Steven J Boege

In a method for measuring luminescence of a biological sample utilizing two different luminescence reagents, the sample is agitated to improve mixing with the second luminescence reagent, allowing for a shorter delay time between injection of the second reagent and measurement of the resulting luminescence activity. The improved mixing may also allow for a shorter measurement time, thereby improving throughput when assaying a large number of samples.

Luminescence measurement of biological samples utilizing dual reagents

A sample analyzing apparatus for performing an optical-based measurement on a sample includes a housing, a first light source, excitation optics, a first light detector, emission optics, and a monitoring system, all of which are disposed in the housing. The monitoring system is configured for monitoring a movable component disposed in the housing. The monitoring system includes one or more light sources for illuminating the movable component, and one or more light detectors for detecting light reflected from the movable component in response to being illuminated.

System for optically monitoring operating conditions in a sample analyzing apparatus

A microplate reader and a method for operating the microplate reader are disclosed. The microplate reader includes a housing, a first NFC reader/writer, a filter tray positioning device, a filter tray, an optical filter disposed in the filter tray, and a controller. The filter tray has a filter tray NFC tag disposed thereon and the filter has a filter NFC tag disposed thereon. The controller receives information about an assay protocol to be undertaken, wherein the assay protocol specifies a filter to be used. The first NFC reader/writer reads filter information stored in the filter NFC tag, the controller directs the NFC reader/writer to store the filter information in the filter tray NFC tag, and the controller enables operation of the microplate reader to undertake the assay protocol only if filter information indicates that the optical filter is in accordance with the filter specified in the assay protocol.

System and method for operating a microplate reader

In a sample analyzing apparatus, an injector assembly injects a reagent onto a sample, and luminescent light from the sample is transmitted to a detector. The assembly may be movable toward and away from the sample. The assembly may include one or more needles that communicate with one or more reservoirs supplying reagent or other liquids. The assembly may include a light guide for communicating with the detector. A cartridge may be provided in which the assembly, one or more reservoirs, and one or more pumps are disposed. The cartridge and/or the apparatus may be configured for enabling rinsing or priming to be done outside the apparatus. The cartridge and/or the apparatus may include one or more types of sensors configured for detecting, for example, the presence of liquid or bubbles in one or more locations of the apparatus and/or the cartridge.

Liquid and plate sensors for microplate injector system

A system is provided for performing filter-based and monochromator-based measurements. The system includes a light source and a plurality of detectors. An excitation monochromator outputs a selected wavelength component of the excitation light. Emitted light from a sample follows a selected emission optical path. An emission monochromator outputs a selected wavelength component of the emitted light when part of the selected path. An interface cartridge includes emission light ports positioned to direct the emitted light from the sample along a corresponding optical path. The interface cartridge aligns a selected optical path with the main measurement optical axis. A movable sliding switch mechanism provides optical channels corresponding to positions on the sliding switch mechanism to complete a selected emission optical path. The position on the sliding switch mechanism is selected by moving the sliding switch mechanism to align the optical channel for the position with the main measurement optical axis.

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Salzburg, Austria

Georg Kronberger