The present invention provides devices and systems for use at the point of care. The methods devices of the invention are directed toward automatic detection of analytes in a bodily fluid. The components of the device are modular to allow for flexibility and robustness of use with the disclosed methods for a variety of medical applications.

Provided is an analysis apparatus having a control part having a preparatory action setting part for determination of whether the first and second controls are performed or the third and fourth controls are performed. The first control sets a sleep-planned part to a sleep state at a first time point when the state of non-use of the analysis apparatus has lasted for a predetermined time length, and then causes performance of a preparatory action by a first predetermined part; the second control resumes the operation of the analysis apparatus when a command signal to resume the operation is received; the third control places a sleep-planned part in a sleep state at a second time point when the state of non-use has lasted for a time length; and the fourth control causes a preparatory action of a second predetermined part to resume operation.

The present invention relates, in part, to systems configured to obtain samples from an organism in an autonomous manner. Such systems can employ a cartridge configured to provide bait to attract an organism, as well as channels to store and/or test samples obtained from the organism.

The present invention provides a detection device of dot immunoblotting detection, including a negative pressure suction device, a hole plate, a hose for connecting the hole plate with the negative pressure suction device, and a nitrocellulose membrane in tight fit with the upper end surface of the hole plate. The present invention further provides a detection method of dot immunoblotting detection, including preparation, sample injection, blocking, incubation of a primary antibody, incubation of a secondary antibody, development and analysis. The detection method performs negative pressure suction through the negative pressure suction device, which is favorable for concentrating samples during sample injection and avoiding the influence, caused by cross contamination after diffusion of the samples, on an experimental result, and the experimental result is more accurate.

The present disclosure relates to systems and methods for determination of analyte concentrations in solution using materials that are pre-dispensed and dried on conjugate pads or other solid substrates. The solution including the analyte can reconstitute the dried material within a vial to produce a specified concentration of material in the vial. The resulting solution can be used in lateral flow testing.

The present invention relates to an immunoassay method and an immunoassay device.

According to an aspect of the present invention, provided is an immunoassay device including: a stage capable of accommodating a plurality of cartridges having a plurality of wells; a solution transfer unit including a plurality of tips, which are movable relative to the stage and disposed to correspond to a position of the cartridge so as to suction a solution stored in each of the wells or discharge the suctioned solution from the well; and a control unit controlling the stage and the solution transfer unit to be relatively movable and controlling suction or discharge of a content into/from the plurality of tips.

A micro-plate reader for use with a portable electronic device having a camera includes an opto-mechanical attachment configured to attach/detach to the portable electronic device and includes an array of illumination sources. A slot in the opto-mechanical attachment is dimensioned to receive an optically transparent plate containing an array of wells. Optical fibers are located in the opto-mechanical attachment and transmit light from each well to a reduced size header having, wherein the fiber array in the header has a cross-sectional area that is ≤10× the cross-sectional area of the wells in the plate. A lens located in the opto-mechanical attachment transmits light from the header fibers to the camera. Software executed on the portable electronic device or other computer is used to process the images to generate qualitative clinical determinations and/or quantitative index values for the separate wells.

The particle is a particle including, in a surface layer thereof, a copolymer having a repeating unit A having a side chain A having, at a terminal thereof, a carboxy group to be bonded to a ligand and a repeating unit B having a side chain B having a hydroxy group at a terminal thereof, wherein when the particle is dispersed in ion-exchanged water, the surface layer of the particle is hydrated to form a swollen layer, wherein the density of the carboxy groups to be incorporated into the swollen layer satisfies a value of from 0.04 group/nm.sup.3 to 0.15 group/nm.sup.3, and wherein the ratio of a particle diameter in water to be measured when the particle is dispersed in ion-exchanged water to a dry particle diameter to be measured when the particle is dried satisfies a value of from 1.10 to 1.40.

The present disclosure provides compositions, methods, systems, and devices for polynucleotide processing and analyte characterization from a single cell. Such polynucleotide processing may be useful for a variety of applications. The compositions, methods, systems, and devices disclosed herein generally describe barcoded oligonucleotides, which can be bound to a bead, such as a gel bead, useful for characterizing one or more analytes including, for example, protein (e.g., cell surface or intracellular proteins) and chromatin (e.g., accessible chromatin).

According to an aspect of the present invention, provided is an immunoassay device including: a control unit controlling relative movement of a stage, which accommodates a cartridge having a plurality of wells, and a solution transfer unit including a tip and the suction and discharge of a solution into/from the tip, wherein the solution transfer unit includes: a driving part providing a pressure for suctioning and discharging the solution into/from the tip; and a magnetic force applying part installed at one side of the tip to apply magnetic force toward the tip, wherein the control unit controls the driving part so that a magnitude of the magnetic force applied to the tip by the magnetic force applying part is adjusted to hold magnetic particles inside the tip after the solution containing the magnetic particles is suctioned into the tip.