A gas analysis device includes a light source configured to emit laser beam to a target gas, a reflection body which reflects the laser beam, a light reception device that receives the laser beam reflected by the reflection body, a container which contains the light source and the light reception device, and an alignment mechanism that includes an insertion member inserted from outside of the container to inside of the container to move, along a plane intersecting with the irradiation direction of the laser beam, at least any one of the light source and the light reception device.

A controller includes a specifying part and a reception part. The specifying part specifies positions where the illumination units are connected. The reception part presents a lightable area and an unlightable area in different modes based on the positions where the illumination units are connected, the positions being specified by the specifying part. The reception part receives settings of the lighting conditions for the lightable area.

An illumination device includes illumination units for irradiating light on an object and a substrate member, which is an example of a holding mechanism for detachably holding the illumination units according to a predetermined disposition rule. The substrate member has a connection part for electrically connecting with a controller. The substrate member holds a part of the illumination units by linking parts.

The present invention relates to a gas sensor (100) comprising a measurement chamber (102) for measuring presence of a first gas, the first gas being nitrous oxide (N.sub.2O) and an optical source (103) for emitting radiation in the measurement chamber (102). The sensor also comprises a radiation detector (104) sensitive to radiation emitted by the optical source (103), the radiation being detected by the radiation detector (104) following passage through the measurement chamber (102). A diffusion layer (131) is configured to allow diffusion of ambient gas into and out from the measurement chamber (102), and the diffusion layer (131) comprises means (133) for preventing diffusion of carbon dioxide (CO.sub.2) in the ambient gas into the measurement chamber (102). The invention also relates a nitrous oxide detector comprising such a gas sensor, and a method for determining presence of nitrous oxide in the ambience.

The present invention is directed to a novel method to multiplex long lifetime fluorescent dyes using time-resolved fluorescence (TRF) detection. A combination of spectral and temporal differences in fluorescence emission is used to enhance the ability to separate signals in an assay from multiple dyes. Multiplexed TRF detection apparatuses and systems configured for performing all or part of any of the methods disclosed herein are also provided, particularly apparatuses and systems incorporating cartridge-based multi-mode readers.

Modular photoacoustic detection device comprising: a photoacoustic cell including at least two chambers connected by at least two capillaries and forming a Helmholtz type differential acoustic resonator; acoustic detectors coupled to the chambers; a light source capable of emitting a light beam having at least one wavelength capable of exciting a gas intended to be detected and which can be modulated to a resonance frequency of the photoacoustic cell; a first photonic circuit optically coupling the light source to an input face of a first of the chambers; wherein the first photonic circuit is arranged in a detachable manner in a first housing formed in the acoustic cell and emerging on the input face of the first chamber.

An inspection apparatus is provided that comprises an optical target including a solid host material and a fluorescing material embedded in the solid host material. The solid host material has a predetermined phonon energy HOST.sub.PE. The fluorescing material exhibits a select ground energy level and a target excitation (TE) energy level separated from the ground energy level by a first energy gap corresponding to a fluorescence emission wavelength of interest. The fluorescing material has a next lower lying (NLL) energy level relative to the TE energy level. The NLL energy level is spaced a second energy gap FM.sub.EG2 below the TE energy level, wherein a ratio of the FM.sub.EG2/HOST.sub.PE is three or more.

Analyte collection and testing systems and methods, and more particularly to disposable oral fluid collection and testing systems and methods. Described herein are methods and apparatuses to achieve significant improvements in the detection of fluorescence signals in the reader.

Systems are provided for a modular multi-wavelength UV-VIS detector unit, such as an absorbance detector (e.g., spectrophotometer) included in a high-performance liquid chromatography system. In one example, a detector unit includes one or more light emitters and a sliding assembly configured to slidingly move a flow cell relative to the one or more light emitters, the one or more light emitters mounted on a floating rig to facilitate alignment between the one or more light emitters and the flow cell when the sliding assembly is in a closed position.

A test element for a mobile water analyzing system includes a sample line and a key reagent disposed in the sample line. The sample line includes an inlet opening arranged at a first end, a pump port arranged at a second end of the sample line, an inlet section arranged between the inlet opening and the pump port, and a measuring section with at least one window arranged at an end of the measuring section. The inlet opening receives a water sample. The measuring section is arranged between the inlet section and the pump port and is coincident with a sample pathway.