Abstract: To provide a microchip that is easily handled. Provided is a microchip having a plate shape and including: a sample liquid inlet into which a sample liquid is introduced; a main flow path through which the sample liquid introduced from the sample liquid inlet flows; and a sorting flow path into which a target sample is sorted from the sample liquid, in which the sample liquid inlet and a terminal end of the sorting flow path are formed on a same side surface. Furthermore, a sample sorting kit including the microchip is also provided. Moreover, a microparticle sorting device on which the microchip is mounted is also provided.

Abstract: To provide a technology of efficiently and effectively sorting microparticles to be sorted from a sample solution. The present technology provides a control device being a device that controls a processing condition when sorting microparticles from a sample liquid flowing through a flow path, the control device provided with a control unit that controls a sorting processing condition on the basis of a content of microparticles to be sorted in the sample liquid. In the control device according to the present technology, the control unit may control the sorting processing condition on the basis of a surviving rate and/or an activation rate of biological particles to be sorted with respect to the sorting processing condition.

Abstract: To provide a technique for controlling a timing for sorting, in order to improve sorting performance of particles in a technique for sorting target fine particles in a passage. Provided is a sorting control device including a sorting control unit configured to adjust a parameter for determination of a sorting condition on the basis of at least one of information regarding a target degree of purity or information regarding a target yield, of a target particle in acquired particles, in a sorting method for sorting a particle flowing through a passage. Furthermore, provided is a particle sorting device for sorting a particle flowing through a passage.

Abstract: According to some aspects, a sample isolation kit is provided. The sample isolation kit includes a housing configured to detachably couple to a sample fluid channel of a microchip and provide a sample to the microchip. The housing and the microchip are coupled using a hermetic seal. The sample isolation kit further includes a storage housing configured to detachably couple to an isolation channel of the microchip and receive a target biological sample isolated from the sample by the microchip. The storage housing and the microchip are coupled using a hermetic seal.

Abstract: There is provided a microchip comprising: a main flow path through which a liquid containing microparticles flows; and a branch flow path that branches from the main flow path. A cross-sectional area of a portion of the main flow path is substantially constant up to a branch start position or decreases toward the branch start position, and a radius of curvature R of a side wall that connects a side wall of the main flow path and a side wall of the branch flow path is 0.5 mm or less and more than 0 mm.

Abstract: There is provided a microchip comprising: a main flow path through which a liquid containing microparticles flows; and a branch flow path that branches from the main flow path. A cross-sectional area of a portion of the main flow path is substantially constant up to a branch start position or decreases toward the branch start position, and a radius of curvature R of a side wall that connects a side wall of the main flow path and a side wall of the branch flow path is 0.5 mm or less and more than 0 mm.

Abstract: To provide a technology of efficiently and effectively sorting microparticles to be sorted from a sample solution. The present technology provides a control device being a device that controls a processing condition when sorting microparticles from a sample liquid flowing through a flow path, the control device provided with a control unit that controls a sorting processing condition on the basis of a content of microparticles to be sorted in the sample liquid. In the control device according to the present technology, the control unit may control the sorting processing condition on the basis of a surviving rate and/or an activation rate of biological particles to be sorted with respect to the sorting processing condition.

Abstract: To provide a technology that enables an upstream particle sorting portion and a downstream particle sorting portion in one microparticle sorting flow channel unit to be controlled independently of each other. The present technology provides a microparticle sorting flow channel unit including: a first particle sorting portion; a fluid storage container that is downstream of the first particle sorting portion and is enabled to store a fluid; and a second particle sorting portion that is downstream of the fluid storage container, in which the fluid storage container is fluidly connected to at least one fluid discharge port that is downstream of the first particle sorting portion and at least one fluid supply port that is upstream of the second particle sorting portion, and the fluid storage container is configured to cause a fluid storage capacity in the container to change depending on a difference between flow rates before and after the container.

Abstract: In embodiments, there is provided a cartridge comprising a container comprising an opening and a holding portion to hold a sample and/or a reagent, an electrode disposed on a container wall of the container, and a removable separator to separate at least some of the holding portion of the container from the electrode when the removable separator is inserted into the holding portion. The cartridge may be combined in a kit with a member to insert the sample, or in an electrical measuring apparatus comprising a circuit to measure electrical characteristic(s) of a second signal, resulting from application of a first signal to the electrode, and indicative of electrical characteristic(s) of the sample and/or the reagent.

Abstract: A technology capable of preventing a sample from being retained is to be provided. Provided are a microchip (1) that includes at least: a sample inlet (11) into which a sample is introduced; a sample flow path (12) through which the sample introduced from the sample inlet (11) flows; and a sorting flow path (16) in which a target sample is sorted out from the sample, in which a first tube (T1) is inserted into and fixed to the sample inlet (11), and a sample sorting kit that includes at least the microchip (1).

Abstract: There is provided an electrical measuring container of a biological sample in a liquid phase, including at least a biological sample holding section that accommodates a biological sample in a liquid phase and made of a resin, and an electrical conductive section fixed to the biological sample holding section. In a state in which a portion of the electrical conductive section is buried in the biological sample holding section, the biological sample holding section and the electrical conductive section are integrally formed with each other.

Abstract: A method of extracting microparticles by detecting target microparticles for extraction in a main flow path which communicates with a pressure chamber, generating for each of the detected target microparticles a change in a negative pressure in the pressure chamber communicating with the main flow path to separate and extract each of the detected target microparticles flowing in the main flow path into the pressure chamber, wherein generating the change of the negative pressure to extract the detected target microparticles comprises generating a negative change in pressure by a different amount in accordance with a separation between the detected target microparticles.

Abstract: A blood state evaluation device, blood state evaluation system, blood state evaluation method, and program that enable evaluation of the risk of thrombosis easily and precisely is provided. An electrical characteristic of blood being an evaluation target is chronologically measured in two or more frequencies or two or more frequency bands. On the basis of chronological change data of the measured electrical characteristic of the blood, a state of blood is evaluated.

Abstract: There is provided a blood condition analyzing device including an erythrocyte quantitative evaluation unit configured to evaluate a hematocrit value and/or a hemoglobin amount on the basis of an electrical characteristic of a blood sample at a frequency of 2 to 25 MHz.

Abstract: Provided is an electrical measuring cartridge including at least: a biological sample holding section that accommodates a liquid biological sample containing a sedimenting component; a measuring electrode unit that is fixed to the biological sample holding section and composed of a pair of electrodes for electrically measuring a state of the biological sample; and a sedimentation measuring electrode unit that is fixed to a position at a different height from the measuring electrode unit of the biological sample holding section and composed of a pair of electrodes for electrically measuring a degree of sedimentation of the sedimenting component.

Abstract: The present technology provides a technology capable of performing stable liquid feeding. For this, the present technology provides a cell sample liquid feeding bag or the like including at least: an outflow port from which cell sample liquid flows out; a bottom portion including a reservoir unit capable of reserving cells and at least partly including a slope; and a first inner tube extending from the outflow port toward the reservoir unit to a position not contacting the reservoir unit, and the cell sample liquid is fed from a reservoir unit side toward an outflow port side of the first inner tube.

Abstract: There is provided an electrical measuring container of a biological sample in a liquid phase, including at least a biological sample holding section that accommodates a biological sample in a liquid phase and made of a resin, and an electrical conductive section fixed to the biological sample holding section. In a state in which a portion of the electrical conductive section is buried in the biological sample holding section, the biological sample holding section and the electrical conductive section are integrally formed with each other.

Abstract: There is provided a microchip comprising: a main flow path through which a liquid containing micro articles flows; and a branch flow path that branches from the main flow path. A cross-sectional area of a portion of the main flow path is substantially constant up to a branch start position or decreases toward the branch start position, and a radius of curvature R of a side wall that connects a side wall of the main flow path and a side wall of the branch flow path is 0.5 mm or less and more than 0 mm.

Abstract: [Solving Means] A flow channel device includes a vessel layer and a flow channel layer. The vessel layer includes an injection vessel section into which a fluid including a sample is injected and a collection vessel section that collects the fluid. The flow channel layer includes a flow channel connected to the injection vessel section and the collection vessel section and is bonded to the vessel layer.

Abstract: There is provided an electrical measuring container of a biological sample in a liquid phase, including at least a biological sample holding section configured to accommodate a biological sample in a liquid phase and made of a resin, and an electrical conductive section fixed to the biological sample holding section. In a state in which a portion of the electrical conductive section is buried in the biological sample holding section, the biological sample holding section and the electrical conductive section are integrally formed with each other.