Provided are methods and systems for reducing the time needed for sequencing nucleic acids. The approach relies on detecting formation of nucleotide-specific ternary complexes comprising a polymerase (e.g., a DNA polymerizing enzyme), a primed template nucleic acid molecule, and a nucleotide complementary to the templated base of the primed template nucleic acid. The methods and systems facilitate determination of the next correct nucleotide, as well as the subsequent next correct nucleotide from a cycle of examining four different nucleotides without requiring chemical incorporation of any nucleotide into the primer.

The present invention relates to an immunoaffinity device for capturing, isolating and purifying one or more analytes of interest present at high or low concentration in simple or complex matrices. The device is designed as an integrated modular unit that includes one or more analyte concentrator-microreactor devices anchored into a T-shaped support box, which is built-in or connected to a interchangeable cartridge-cassette of a capillary electrophoresis or liquid chromatography apparatus for the isolation, enrichment, derivatization, separation and characterization of small molecules and polymeric macromolecules, primarily protein and peptide biomarkers. The integrated modular unit is also designed to perform metabolic or bioactivity studies.

Methods and apparatus for detecting, quantifying, enriching, and/or separating bacterial species in fluid sample are provided. The fluid sample is provided as input to a microfluidic passage of a microfluidic device, wherein the microfluidic device comprises at least one electrode disposed adjacent to the microfluidic passage. The at least one electrode is activated to capture bacteria in the sample using dielectrophoresis, wherein the capture efficiency of bacteria is at least 99%.

The present disclosure provides a method for performing agglutination assays on a “two plate” DMF device format. Droplets containing analytes of interest (particles, cells, etc.) are loaded into the DMF device and mixed with solution-phase or dried agglutinating antibodies or antigens. The agglutinating agents bind to their complementary targets (e.g. antibodies or antigens for example) in the sample droplets, which leads to the formation of insoluble aggregates. Active mixing on a DMF device reduces the reaction time and enhances the agglutination effect. Since the agglutinated sample is sandwiched between two plates on the DMF device, it is straightforward to visualize the result by eye or via a digital camera.

In an example, a target material is immobilized on two opposed sequencing surfaces of a flow cell using first and second fluids. The first fluid has a density less than a target material density and the second fluid has a density greater than the target material density; or the second fluid has a density less than the target material density and the first fluid has a density greater than the target material density. The first fluid (including the target material) is introduced into the flow cell, whereby at least some of the target material becomes immobilized by capture sites on one of the sequencing surfaces. The first fluid and non-immobilized target material are removed. The second fluid (including target material) is introduced into the flow cell, whereby at least some of the target material becomes immobilized by capture sites on another of the sequencing surfaces.

A device for collecting particles present in a gas or gas mixture, including a component, a collection zone disposed on the component, on which said particles are deposited, collection device configured to force said particles to be deposited against the collection zone, a fluidic elution circuit arranged in said component to elute the particles present in the collection zone.

Some embodiments described herein relate to a method that includes separating an analyte-containing sample via electrophoresis in a capillary. The capillary is loaded with a chemiluminescence agent, such as luminol, that is configured to react with the analyte (e.g., HRP-conjugated proteins) to produce a signal indicative of a concentration and/or quantity of analyte at each location along the length of the capillary. A first image of the capillary containing the analytes and the chemiluminescence agent is captured over a first period of time. A second image of the capillary containing the analytes and the chemiluminescence agent is captured over a second, longer, period of time. A concentration and/or quantity of a first population of analytes at a first location is determined using the first image, and a concentration and/or quantity of a second population of analytes at a second location is determined using the second image.

The present invention discloses a pathogenic microorganisms rapid concentration device and method. The device comprises an electrode and a microchannel for passing a sample, wherein the microchannel comprises a concentration channel and a sample channel, between which a filter element is provided, the electrode comprises a positive electrode and a negative electrode, the positive electrode comprises several sub-positive electrodes, after the sample flows into the microchannel, under the action of the electrode, pathogenic microorganisms in the sample are regionally enriched on a positive electrode side of the concentration channel to form a concentrated sample. The present invention provides a substantial increase in the rate and efficiency of purification of samples containing pathogenic microorganisms through precise electrical control. The concentration of pathogenic microorganisms can be achieved accurately and efficiently by controlling the voltage applied by the sub-positive electrode, which provides a good basis for the integration, automation, rapid and continuous sampling, and detection.

Provided is a target substance detection device that can detect a target substance accurately and efficiently and can be manufactured at low costs. A target substance detection device 10 includes: a liquid sample storage unit 15 that is partially or wholly formed of a transparent member, and includes a storage unit formed so as to be open at a top surface thereof and configured to store a liquid sample S containing a fluorescent substance and magnetic particles that form a conjugate with a target substance; a sensing plate 11 composed of a silicon flat plate whose bottom surface is a smooth surface, the bottom surface being joined to the top surface of the liquid sample storage unit 15; a light irradiation unit 12 configured to irradiate the bottom surface of the sensing plate 11 with light including an excitation wavelength of the fluorescent substance, via the liquid sample storage unit 15; and a magnetic field application unit 14 located on a top surface side of the sensing plate 11, and configured to move a permanent magnet in a direction having a vector component in a direction parallel to an in-plane direction of the bottom surface of the sensing plate 11 in a state in which a magnetic field is applied to the conjugate in the liquid sample S stored in the storage unit.

A fluid entrained particle separator may include an inlet passage to direct particles entrained in a fluid, a first separation passage branching from the inlet passage, a second separation passage branching from the inlet passage and electrodes to create electric field exerting a dielectrophoretic force on the particles to direct the particles to the first separation passage or the second separation passage, wherein the first separation passage, the second separation passage, the electric field and the dielectrophoretic force extend in a plane.