A flow cell has: a flow path in which a specimen fluid and a sheath fluid flow; a specimen flow path that introduces the specimen fluid into the flow path; a first sheath flow path and a second sheath flow path that introduce the sheath fluid into the flow path; and a merging portion at which the specimen flow path, the first sheath flow path and the second sheath flow path merge together. The specimen flow path is provided on a central flow line of the flow path. At the merging portion, the first sheath flow path and the second sheath flow path face directions intersecting the central flow line of the flow path, and are disposed at positions that are offset in a depth direction of the flow path.

The disclosure relates to a flow cytometer arrangement, in which a sample is mixed with a colorant by means of two pumps and the mixture is introduced together with a sheath flow into a flow cell.

The present invention provides microfabricated substrates and methods of conducting reactions within these substrates. The reactions occur in plugs transported in the flow of a carrier-fluid.

Microfluidic devices and methods for focusing components in a fluid sample are described herein. The microfluidic device has at least one flow focusing channel where the components are focused or re-oriented by the geometry of the channel. From an upstream end of the flow focusing channel to a downstream end of the flow focusing channel, at least a portion of the flow focusing channel has a reduction in height and at least a portion of the flow focusing channel narrows in width, thereby geometrically constricting the flow focusing channel. The devices and methods can be utilized in sex-sorting of sperm cells to improve performance and increase eligibility.

An impedance cytometry device is described along with methods of accurately measuring particle size of particles contained in a fluid that is passed through the impedance cytometry device. The impedance cytometry device includes a substrate, and an electrode arrangement deposited on the substrate in a co-planar fashion. The electrode arrangement includes a drive electrode and a plurality of measurement electrodes located in a same plane as the drive electrode. The plurality of measurement electrodes includes at least two pairs of measurement sub-electrodes, each pair of measurement sub-electrodes including a first measurement sub-electrode positioned adjacent to the drive electrode, and a second measurement sub-electrode separated from the drive electrode by a respective first measurement sub-electrode. The impedance cytometry device may be incorporated into a substrate assembly of an electrowetting on dielectric (EWOD) device, such as in a substrate assembly containing electrowetting drive electrodes or a common reference electrode, or into a microfluidic blood counter device.

A microfabricated sheath flow structure for producing a sheath flow includes a primary sheath flow channel for conveying a sheath fluid, a sample inlet for injecting a sample into the sheath fluid in the primary sheath flow channel, a primary focusing region for focusing the sample within the sheath fluid and a secondary focusing region for providing additional focusing of the sample within the sheath fluid. The secondary focusing region may be formed by a flow channel intersecting the primary sheath flow channel to inject additional sheath fluid into the primary sheath flow channel from a selected direction. A sheath flow system may comprise a plurality of sheath flow structures operating in parallel on a microfluidic chip.

There is provided a connecting member to be attached to a substrate that includes at least a sample introduction section to introduce a sample, a sheath liquid introduction section to introduce a sheath liquid, and a jetting section to jet droplets, the connecting member including at least: a sample introduction linking section to be linked to the sample introduction section; a sheath liquid introduction linking section to be linked to the sheath liquid introduction section; and a charging electrode section that provides charges to at least part of the droplets. The sample introduction linking section and the sheath liquid introduction linking section are positioned so as to be linked to corresponding positions of the substrate.

A fluid delivery method for delivering a liquid sample to a flow cell including a taper section including a first and a second inner walls opposing the first inner wall, which is inclined to the second inner wall so that a distance between the first and the second inner walls at a downstream side of the taper section is shorter than a distance at an upstream side of the taper section, and including measurement flow path provided downstream of the taper section, through which a liquid sample flows together with a sheath fluid. The fluid delivery method includes sample introduction of delivering the liquid sample into the taper section along the second inner wall until the liquid sample reaches the measurement flow path, and sample pressing by delivering the sheath fluid into the taper section along the first inner wall after the liquid sample reaches the measurement flow path.

A liquid sample analysis method including communicating a specific flow path with an aspirator via a branch flow path, aspirating air from the aspirator, aspirating a liquid sample into the sample supply path from the aspirator so that an entire amount of the aspirated air is accommodated in the branch flow path, communicating a sample extrusion path with a sample port, communicating a sheath fluid supply path with a sheath fluid port, and isolating the branch flow path from both the sample supply path and the specific flow path, extruding the liquid sample in the sample supply path so as to inflow into the sample flow path by causing a sheath fluid to inflow into the sheath fluid flow path from the sheath fluid supply path and causing the sheath fluid to inflow into the sample supply path from the sample extrusion path.

A sheath flow impedance particle analyzer includes a pre-mixing cell, a sample needle, a sheath flow impedance counting cell, a front sheath fluid cell, a rear sheath fluid cell, a rear sheath waste fluid cell, a waste fluid cell, and a first auxiliary negative pressure source. The first auxiliary negative pressure source includes at least one low pressure port, and a valve for controlling the low pressure port to open or close, the low pressure port being connected to the sample needle or the rear sheath waste fluid cell. During measurement of a sample by the sheath flow impedance counting cell, at least the negative pressure of the first auxiliary negative pressure source enables the sample needle to transfer a sample liquid or enable the rear sheath waste fluid cell to discharge a waste fluid.