An analysis device that includes a placement section, a pressing member, and a measurement member, has an analysis kit including a chip provided with a capillary through which a sample flows and a cartridge superimposed on the chip, and in which a liquid reservoir placed therein to enable a component present in sample can be measured in a state in which the chip and the cartridge have been fitted together. The analysis kit is placed on the placement section. The pressing member presses the analysis kit in a direction in which the cartridge is superimposed on the chip to sandwich the analysis kit between the pressing member and the placement section, and to fit the chip and the cartridge together. The measurement member that measures the component present in the sample in the analysis kit in which the chip and the cartridge have been fitted together.

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.

A fluidic assembly comprising a fluid analysis apparatus (30), the fluid analysis apparatus (30) comprising: a fluid measurement device (34); a fluidic device including a flow cell (36) arranged in a measurement region of the fluid measurement device (34), the flow cell (36) constructed of at least one first fluoropolymer material, the flow cell (36) including a channel, the channel containing a sample segment (52) that is carried in a fluorinated fluid carrier (54), wherein the sample segment (52) and fluorinated fluid carrier (54) are immiscible.

Methods and systems are provided for the identification of sample cells in a sample tray that is placed in a chromatography autosampler. A cell gripper and labels are also provided to facilitate such identification.

A sample collection and testing device for analyzing blood is provided that includes a controller, a fluid flow pathway, a pump configured to move fluid through the fluid pathway, and an optical fluid measurement element configured to measure a light intensity of the fluid in the fluid flow pathway. The controller is configured to: start the pump to move a blood sample in the fluid flow pathway, receive a signal from the optical fluid measurement element indicating a detection of a leading edge of the blood in the fluid flow pathway, stop the pump to stop the moving of the blood in the pathway, receive a plurality of light intensity measurements from the optical measurement element, each light intensity measurement measured at a corresponding point of time, and provide a mapping of the light intensity measurements into an indication of a coagulation of the blood sample over a time period.

A device for analyzing a gaseous sample including a first housing including a detection assembly housed in the housing including a preconcentrator, a chromatography column and a detector intended to detect the presence of the separated compounds, a sampling assembly including a cartridge that is removable relative to the first housing, a control and processing unit housed in the housing and configured to execute an analysis operating mode capable of generating a first command for the detection assembly to analyze a first gaseous sample, a second command to determine the exceeding of at least one alert threshold and, if an alert threshold is exceeded, a third command for the sampling assembly to take a second gaseous sample.

A method for collecting and delivering biological samples to a destination, such as an analyzer are provided herein. In one example, a plurality of samples, each including particles, is obtained from respective wells of a sample source having a plurality of wells. The plurality of samples are introduced into a fluid flow stream contained within a conduit having an inner diameter and in communication with a destination. An inner surface of the conduit is coated with a hydrogel barrier substance, such as poly-HEMA. The fluid flow stream is guided through the conduit to a destination. In one example, the destination may be a flow cytometer. Methods of preparing a poly-HEMA solution and coating the inner surface of a conduit with poly-HEMA are also provided.

An electronic microscope includes a carrier, a first driving unit, a flow-buffer unit and an electron source. The carrier carries a sample. The first driving unit drives a first fluid to flow along a first flow path, wherein the first flow path passes through the sample. The flow-buffer unit is disposed on the first flow path to perform buffering on the first fluid, wherein the first fluid flows through the flow-buffer unit and the carrier in sequence. The electron source provides an electron beam to the sample.

The invention provides systems, compositions, kits and methods for automated processing of biological samples and analysis using a flow cytometer.

A computer-implemented method for spectroscopic analysis of biological material is provided that includes analyzing samples of biological material from a plurality of sources, and delivering samples of biological material to at least one flow cell for spectroscopy, and determining whether the spectroscopic analysis for each sample of the plurality of samples is or is predicted to be ambiguous in that it is affected by at least two non-discriminable factors. If such a determination is made, a disambiguating step can be performed.