A cuvette for analysis of liquids, including a first cuvette portion and a second cuvette portion, which are joined together, with a cuvette cavity, an inlet passage and an outlet passage being formed between the first cuvette portion and the second cuvette portion, the inlet passage and the outlet passage both in communication with the cuvette cavity, wherein the outlet passage is provided therein with a labyrinth-like sealing structure, which prevents backfill of a gas that has been discharged from the outlet passage during filling of a liquid to be analyzed in the cuvette.

This invention relates to retrievable measuring cell for optical measurements in gas, the cell being defined by a gas conducting pipe having an input end adapted to be connected to a gas flow input intruding gas into the cell and an output end adapted to be connected to a gas flow output. The pipe ends also being adapted to be coupled to optical components including an optical transmitter transmitting light into said cell and an optical receiver adapted to receive light having passed through said cell, the optical beam in said cell having a predetermined shape, the optical components including a light source, at least two minors and a light receiver being mounted in known positions on an external frame covered by the pipe ends. The cell has an elongated shape corresponding to the optical beam shape.

Apparatuses, systems, and methods for Raman spectroscopy are described. In certain implementations, a spectrometer is provided. The spectrometer may include a plurality of optical elements, comprising an entrance aperture, a collimating element, a volume phase holographic grating, a focusing element, and a detector array. The plurality of optical elements are configured to transfer the light beam from the entrance aperture to the detector array with a high transfer efficiency over a preselected spectral band.

A method can be provided for analyzing a fluidic sample with dispersed particles. Using such exemplary method, it is possible to irradiate the sample with light, so that the photons of the light transfer momentum to the particles. It is also possible to measure at least one property of the particles that is altered by the momentum transfer. The light can be a propagating beam with an intensity distribution that has gradients pointing to more than one point within each plane normal to the direction of propagation, while varying steadily along the direction of propagation, and/or a 3D vortex trap beam that is configured to confine the particles in a three-dimensional volume by means of high-intensity gradients. An exemplary device can also be provided (e.g., for performing the method), comprising a chamber for holding a sample that is elongate along an axis and configured to pass a beam of light along the axis. The chamber can have a conical inner cross section that substantially expands in the direction of propagation of the beam.

The present invention relates to an apparatus for performing a nucleic acid amplification reaction and a fluorescence detection device for reaction analysis. The nucleic acid amplification apparatus of the present invention uses a plurality of blocks having different reaction temperatures by independent temperature control and the movement between the blocks is performed along sliding recesses formed in the blocks, enabling to greatly shorten the total amplification time (TAT). In the fluorescence detection device of the present invention, the positions of the light source and the photodetector are very unique for the reaction vessel in which an excitation light is provided and an emission light is generated.

A detection method uses a reaction vessel including a container including a housing part having a first opening opened at an upper portion and a second opening opened at a side portion, and a side wall member fixed to the container so that a capturing region on a metal film is exposed in the second opening. First, a liquid containing a specimen is provided to the housing part. Next, the liquid in the housing part is stirred to capture, into the capturing region, a substance to be detected in the liquid. Next, the metal film is irradiated with light so that surface plasmon resonance occurs in the metal film, and light emitted from the reaction vessel and having a light amount changing depending on the amount of the substance to be detected captured in the capturing region is detected. In the step of providing the liquid to the housing part, an amount of liquid in which the liquid is not in contact with the capturing region when the liquid in the housing part is left still, and the liquid is in contact with the capturing region when the liquid in the housing part is stirred is provided to the housing part.

A biological sample reaction vessel comprising a reagent storage portion and a push rod movable relative to the reagent storage portion is provided. The reagent storage portion comprises at least one reagent containing cavity, and the reagent containing cavity is sealed by a sealing element; and the push rod is connected to the sealing element, and the push rod is used for cooperation with an external device to separate the sealing element from the reagent storage portion. In reaction, the biological sample reaction vessel cooperates with a test cassette. By inserting the biological sample reaction vessel into the external device, the reagent in the reagent storage portion can be released rapidly.

Provided is a water examination device including: a main body; a fluid accommodation unit formed in the main body; a wave source for irradiating waves toward the fluid accommodation unit; a detector for detecting a laser speckle at every set time period that is set in advance, the laser speckle being generated due to multiple scattering of the waves in the fluid; a controller for estimating existence of impurities in the fluid in real-time by using the detected laser speckle; and a calibration unit for controlling the wave source or the detector such that an intensity of light irradiated from the wave source and measured by the detector is within a certain range set in advance.

A microfluidic apparatus has a microchannel that includes at least one vertically oriented segment with a top section having a relatively wide opening and a bottom section having a relatively narrow opening. The top section is larger in volume relative to the bottom sections, and the middle sections taper down in at least one dimension from the top section to the bottom section. One or tens or hundreds of vertically-oriented segments may be provided, and they are fluidly coupled to each other. Each segment acts as a pressure-volume-temperature (PVT) cell, and the microchannel apparatus may be used to determine a parameter of a fluid containing hydrocarbons such as the dew point of the fluid or the liquid drop-out as a function of pressure.

A reaction vessel capable of measuring a light amount from a reaction liquid without degrading a function of maintaining the reaction vessel at a predetermined temperature is provided. A reaction vessel including a cylindrical shape centered on a first axis, in which an overall length in a first axis direction is longer than an overall length in a second axis direction and an overall length in a third axis direction, the second axis being perpendicular to the first axis and the third axis being perpendicular to the first axis and the second axis. The reaction vessel includes: an opening part which dispenses a liquid at a portion on one end side in the first axis direction; a first flat surface and a second flat surface which is substantially parallel to the first flat surface.