Abstract: A conveyor system, comprising a first conveyor assembly having: an input end; an output end; and a conveyor belt arranged to convey an object from the input end toward the output end in a direction of travel. The conveyor system comprises a fluid projection mechanism, the fluid projection mechanism being arranged to provide a fluid suitable for providing a lifting force to a conveyed object as the conveyed object passes over the fluid projection mechanism.

Abstract: A conveyor system, comprising a first conveyor assembly having: an input end; an output end; and a conveyor belt arranged to convey an object from the input end toward the output end in a direction of travel. The conveyor system comprises a fluid projection mechanism, the fluid projection mechanism being arranged to provide a fluid suitable for providing a lifting force to a conveyed object as the conveyed object passes over the fluid projection mechanism.

Abstract: Provided are computer-implemented methods for producing an index. The methods include conditioning electroencephalographic (EEG) signals present in an EEG recording previously obtained from an individual, e.g., an individual having dementia. In certain embodiments, the methods further include determining frequency domain features from the conditioned EEG signals, and determining connectivity features from the frequency domain features, where the connectivity features include connectivity features determined from a frequency range of from 35 Hz to 45 Hz divided into two or more sub-bands. The methods further include producing an index calculated at least in part as a function of one or more of the connectivity features determined from a frequency range of from 35 Hz to 45 Hz divided into sub-bands with varying contribution to the calculation of the index. Also provided are computer readable media and computer devices that find use, e.g., in practicing the methods of the present disclosure.

Abstract: Methods for screening libraries of polypeptides for biologically activity on cells. For example, polypeptides can be synthesized and encapsulated along with their coding sequences in microcapsules of an emulsion. Emulsion microcapsules can then be fused with microcapsules comprising test cells and biological activity on the cells is assessed to identify biologically active polypeptides and nucleic acid molecules encoding the same.

Abstract: Methods for screening libraries of polypeptides for biologically activity on cells. For example, polypeptides can be synthesized and encapsulated along with their coding sequences in microcapsules of an emulsion. Emulsion microcapsules can then be fused with microcapsules comprising test cells and biological activity on the cells is assessed to identify biologically active polypeptides and nucleic acid molecules encoding the same.

Abstract: A cell culture device for the study of barrier function and differentiation are provided by this invention.

Abstract: A device and method are disclosed to enable fluid manipulations without disturbing or removing particles or cells. By engineering assay compartment geometries to take advantage of fluid mechanical effects, the flow velocity may be diminished around particles or cells. This technology may be used to process particles or cells of various kinds that are suspended in liquids or gels, and is suitable for use in high throughput screening.

Abstract: A method is provided for pumping fluid through a channel of a microfluidic device. The channel has an input port and an output port. The channel is filled with fluid and a pressure gradient is generated between the fluid at the input port and the fluid at the output port. As a result, fluid flows through the channel towards the output port.

Abstract: This invention relates to a device and method for engineering microchannel geometries to take advantage of surface tension to guide fluid location. This technology may be used to construct compartmentalized systems of various materials that are added in liquid state, and may be used in a liquid state, or may be solidified, gelled, cross-linked, polymerized, or alternatively may be accumulated through gravity (e.g. cell settling), or centrifugation.

Abstract: A device and method is provided for performing a high throughput assay. The device includes a plate structure having a plate and a plurality of microfluidic structures positioned thereon. Each microfluidic structure defines a channel having an input and an output. At least one of the input and the output of the channel of each of the plurality of mircofluidic structures includes a first plurality of ports. In operation, the channels are filled with fluid and pressure gradients are generated between the fluids at the inputs and the fluids at the outputs of the channels. As a result, fluid flows through the channels toward the outputs.

Abstract: A microfluidic method and device for testing and analyzing chemotaxis by providing a stable, static fluid gradient. The device includes a sink reservoir for receiving biological cellular material and a source reservoir for receiving a chemoattractant. The biological cellular material migrates through a low fluid volume microfluidic gradient channel located between the source and sink reservoirs. The fluid in the gradient channel is static and stable due to a high fluid volume closed circuit bypass microfluidic channel also in fluid communication with the source and sink reservoirs, whereby the bypass channel relieves any pressure differential imparted across the gradient channel.

Abstract: A device and method is provided for performing a high throughput assay. The device includes a plate structure having a plate and a plurality of microfluidic structures positioned thereon. Each microfluidic structure defines a channel having an input and an output. At least one of the input and the output of the channel of each of the plurality of mircofluidic structures includes a first plurality of ports. In operation, the channels are filled with fluid and pressure gradients are generated between the fluids at the inputs and the fluids at the outputs of the channels. As a result, fluid flows through the channels toward the outputs.

Abstract: A method is provided of controlling communication between multiple ports in a microfluidic device. The method includes the step of providing a channel network in a microfluidic device. The channel network including a first channel having a first input port and an output port. The first channel is filled with a fluid and a first output droplet is deposited on the output port. The first output droplet has a radius of curvature. The first output droplet flows toward the first input port in response to placement of a first input droplet having a radius of curvature greater than the radius of curvature of the first output droplet on the first input port. The first input droplet flows toward the output port in response to the first input droplet having a radius of curvature less than the radius of curvature of first output droplet.

Abstract: A method of quantifying cell migration of a cell population is provided. The method includes the step of patterning the cell population within a channel network in a first body. A first image of the cell population is obtained. Thereafter, a second image of the cell population is obtained after a first predetermined time period. The first and second images are compared in order to calculate a quantitative measure of the average directional migration of the cells population and a quantitative measure of the average motility of the cell population.

Abstract: A device and method is provided for performing a high throughput assay. The device includes a plate structure having a plate and a plurality of microfluidic structures positioned thereon. Each microfluidic structure defines a channel having an input and an output. At least one of the input and the output of the channel of each of the plurality of mircofluidic structures includes a first plurality of ports. In operation, the channels are filled with fluid and pressure gradients are generated between the fluids at the inputs and the fluids at the outputs of the channels. As a result, fluid flows through the channels toward the outputs.

Abstract: A method is provided for pumping fluid through a channel of a microfluidic device. The channel has an input port and an output port. The channel is filled with fluid and a pressure gradient is generated between the fluid at the input port and the fluid at the output port. As a result, fluid flows through the channel towards the output port.

Abstract: A method is provided for pumping fluid through a channel of a microfluidic device. The channel has an input port and an output port. The channel is filled with fluid and a pressure gradient is generated between the fluid at the input port and the fluid at the output port. As a result, fluid flows through the channel towards the output port.

Abstract: A method is provided for pumping fluid through a channel of a microfluidic device. The channel has an input port and an output port. The channel is filled with fluid and a pressure gradient is generated between the fluid at the input port and the fluid at the output port. As a result, fluid flows through the channel towards the output port.

Abstract: A device and method for conducting peristaltic pumping of a fluid in a body is provided. The body includes a channel having an input and an output and being partially defined by a flexible layer. A plurality of contacts are spaced along the layer and the channel is filled with the fluid. The plurality of spaced contacts is magnetically coupled to a magnetic field in sequence so as to translate peristaltic motion to the layer thereby pumping the fluid through the channel.

Abstract: A microfluidic method and device for testing and analyzing chemotaxis by providing a stable, static fluid gradient. The device includes a sink reservoir for receiving biological cellular material and a source reservoir for receiving a chemoattractant. The biological cellular material migrates through a low fluid volume microfluidic gradient channel located between the source and sink reservoirs. The fluid in the gradient channel is static and stable due to a high fluid volume closed circuit bypass microfluidic channel also in fluid communication with the source and sink reservoirs, whereby the bypass channel relieves any pressure differential imparted across the gradient channel.