Abstract: An automatic sample injection system (1) includes at least an injector (2). The injector (2) includes a turret (10) comprising a plurality of vial receiving holes (30) that are corresponding to a plurality of types of vials having different sizes, the plurality of vial receiving holes (30) being provided on the same circumference on an upper surface of the turret, the turret being configured to rotate so that the plurality of the vial receiving holes (30) are each moved along a circumferential track, and a controller (22) configured, in a case where a sampler (4) for supplying a vial to the injector (2) is provided, to recognize a size of a target vial to be supplied at the time when the target vial is supplied from the sampler (4) and to arrange the vial receiving hole (30) corresponding to the target vial at a delivery position (P) set on the circumferential track.

Abstract: One aspect of the present invention provides a nucleic acid extraction device. The nucleic acid extraction device includes a container which stores each of a cleaning solution and an eluting solution, a water level sensor configured to detect amounts of the cleaning solution and the eluting solution which are stored in the container, a tube sensor configured to sense a sample tube disposed on a sample tube accommodation portion, and an operation initiation portion configured to determine whether the cleaning solution and the eluting solution which are necessary for a nucleic acid extraction operation are provided on the basis of the number of such sample tubes which is sensed by the tube sensor and the amounts of the cleaning solution and the eluting solution which are sensed by the water level sensor.

Abstract: A method and system for performing biomolecule extraction are provided that use liquid-to-liquid extraction (LLE) in combination with an electrowetting on dielectric (EWOD) device to provide a biomolecule extraction solution that has high extraction efficiency and that is less costly and easier to use than current state of the art methods and systems. The system and method are well suited for, but not limited to, extraction of DNA, RNA and protein molecules.

Abstract: A sample collection system can include a sample collection vessel having a sample collection chamber with an opening configured to receive a sample into the sample collection chamber. The sample collection system can additionally include a selectively movable sleeve valve configured to associate with the opening of the sample collection chamber. The sample collection system can include a sealing cap that is configured to associate with the selectively movable sleeve valve and with the sample collection vessel. The sealing cap can include a reagent chamber having reagent(s) stored therein, and when the sealing cap is associated with the sample collection vessel, the selectively movable sleeve valve opens, dispensing the reagent(s) into the sample collection chamber. When the selectively moveable sleeve associates with the sample collection chamber, an outer sleeve slides relative to an inner vessel, opening the sleeve and dispensing reagent into the sample collection chamber.

Abstract: Bead-based analytical assays suitable for detecting changes in the abundance of target analytes in biological samples are disclosed. In an embodiment, an assay involves incubating a sample with one or several beads that are capable of binding several distinct analytes in an amount sufficient for detection by mass spectrometry from a single bead.

Abstract: An autonomous bioaerosol sampling and detection system and method adapted to provide real-time detection and identification of bio-organisms in aerosols without human intervention.

Abstract: The present invention relates to compositions and methods for determining the absolute configuration of D/L-cysteine and/or the enantiomeric composition of cysteine and/or the concentration of total cysteine in a sample. Uses of the composition and method are also described.

Abstract: A method is provided for manipulating objects in a cavity including a liquid, the method including providing in at least one region of the cavity objects capable of absorbing light in a given wavelength range, forming an aggregate of the objects by submitting them to an acoustic field, and disrupting the aggregate by submitting the aggregate to a light beam emitting at the given wavelength range. Also provided is a device for manipulating objects.

Abstract: A liquid handling device includes a plurality of first wells configured for a first sample; a first channel connected to the plurality of first wells; a plurality of second wells configured for a second sample; a second channel connected to the plurality of second wells; a plurality of processing agent wells configured for a processing agent configured to process the first sample and the second sample; a processing agent channel connected to the plurality of processing agent wells; and a common channel connected to the first channel, the second channel and the processing agent channel.

Abstract: Disclosed herein are systems and methods for quantifying analytes in a desired complex solution with minimal inter-sample variability. The invention includes methods and diagnostic tools for quantifying analytes in aqueous solutions or biological fluid samples with sample-specific calibration and colorimetric or detectable output.

Abstract: A container comprising: a first panel; a second panel opposing the first panel; a first side; a second side opposing the first side; a third side; a fourth side opposing the third side; wherein each of the sides joins the first panel and the second panel; a chamber defined by the four sides, the first panel, and the second panel, wherein the chamber is configured to receive a biological specimen; a port defined in the first side; a plug inserted into the port; an opening defined in the second side; and a closure element coupled to the opening, wherein the chamber is leak proof.

Abstract: The present disclosure is directed toward a measurement system capable of rapid spectroscopic and calorimetric analysis of the chemical makeup of a test sample. Systems in accordance with the present disclosure include a low-thermal-mass sample holder having a substrate whose surface has been engineered to create a large-area sample-collection surface. The sample holder includes an integrated temperature controller that can rapidly heat or cool the test sample. As a result, the sample holder enables differential scanning calorimetry Fourier-Transform Infrared Spectroscopy (DSC-FTIR) that can be performed in minutes rather than hours, as required in the prior art.

Abstract: A composition and method for the photometric determination of a film-forming amine in liquid by adding an indicator reagent to an aqueous system that is pH dependent, combining a water soluble non-ionic polymer to modify the physical properties of the aqueous system, and adding an acidic buffer to said aqueous system to lower pH and activate said indicator, said water soluble polymer keeping the filming amine/indicator complex in solution despite the acidic buffer and preventing it from precipitating out.

Abstract: A portable device for measuring the concentration of at least one component in a gas exhaled by a breath fluid, including a first chamber located upstream of a measuring vessel and including an inlet through which the exhaled breath fluid enters the first chamber, a second chamber located upstream of the measuring vessel, the second chamber including an inlet leading into the first chamber, an outlet in communication with the measuring vessel and through which some of the exhaled breath fluid passes, and an outlet leading to the ambient air, through which some of the exhaled breath fluid is expelled into the ambient air. Further, the second chamber is located inside or adjacent the first chamber and the outlet to the ambient air leads to the first chamber so some of the exhaled breath fluid enters the second chamber through the inlet of the second chamber.

Abstract: A microfluidic sample chip to test biological samples, especially for a PCR-type and/or fluorescence assay. The chip being in the shape of a hollow block having at least one chamber delimited by an upper wall, a lower wall and at least one side wall, into which a sample can be introduced for testing. The lower wall of the block is made of a material with a high thermal conductivity and the upper wall is made of a material with a low thermal conductivity. Preferably, the upper wall is preferably permeable to radiation in the visible spectrum between 400 and 700 nm. The block having at least two openings through which the sample can be introduced into at least one of the chambers and through which the air present in the chamber can be evacuated when the sample is introduced.

Abstract: Described herein are systems relating to a continuous-flow instrument that includes all necessary components for digital droplet quantification without the need to introduce key reagents or collect and transfer droplets between stages of instrument operation. Digital quantification can proceed without any additional fluid or consumable handling and without exposing fluids to risk of external contamination.

Abstract: A single junction sorter for a microfluidic particle sorter, the single-junction sorter comprising: an input channel, configured to receive a fluid containing particles; an output sort channel and an output waste channel, each connected to the input channel for receiving the fluid therefrom; a bubble generator, operable to selectively displace the fluid around a particle to be sorted and thereby to create a transient flow of the fluid in the input channel; and a vortex element, configured to cause a vortex in the transient flow in order to direct the particle to be sorted into the output sort channel.

Abstract: A digital microfluidic device, comprising a bottom plate and a top plate. The bottom plate comprises a bottom electrode array comprising a plurality of digital microfluidic propulsion electrodes. The top plate comprises a segmented top electrode array comprising a plurality of separately voltage addressable top electrode segments. Each top electrode segment and at least two of the propulsion electrodes of the bottom electrode array form a zone within the device. A controller is operatively coupled to the top electrode array and to the bottom electrode array and is configured to provide propulsion voltages between the top plate segment and the bottom plate propulsion electrodes of at least one of the zones. The top plate and the bottom plate are provided in a spaced relationship defining a microfluidic region therebetween.

Abstract: A microfluidic test device has a body, a first chamber having an outlet provided with a first valve and holding a first buffer having a first buffer volume, a primary reaction chamber, a sample inlet for receiving and feeding a sample having a sample volume, into the microfluidic test device, a first fluid path connecting the outlet of the first chamber and the sample inlet, a second fluid path connecting the sample inlet and the primary reaction chamber, a primary test part having a primary test chamber, a third primary fluid path connecting the primary reaction chamber and the primary test part, a primary valve arranged in the third primary fluid path, a flow driving device configured to move fluid from the primary reaction chamber to the primary test part, and a heating assembly configured to heat a reaction fluid in the primary reaction chamber.

Abstract: Disclosed is a system and device for determining sex of an embryo utilizing a non-invasive grading of early stage embryos (pre-hatching) based upon specific gravity, density and/or estimated weight. The device comprises a drop chamber having a lumen, capable of assessing characteristics of at least one embryo while descending. The system allows 100% recovery of embryos. A processor is further capable of performing assessment of the embryos. The disclosed system supports a wide variety of scenarios for human and animal reproductive technologies and related products and services.