G01N30/00

METHOD, KIT AND TEST STRIP FOR DETECTING KAWASAKI DISEASE

The present invention provides methods in the context of Kawasaki disease including measuring the level of at least one of lipopolysaccharide binding protein, leucine-rich alpha-2-glycoprotein, angiotensinogen and retinol binding protein 4 in a sample derived from a subject.

Supercritical fluid processing device

A supercritical fluid chromatograph includes a supercritical flow path, a mobile phase supply section for supplying a mobile phase containing liquid carbon dioxide, a sample introduction section, a sample separation section, a detector, and a pressure control valve. A valve post-stage flow path is connected to a fluid outlet of the pressure control valve, and the inside of the valve post-stage flow path is maintained by pressure maintaining means at a pressure by which a mobile phase from the fluid outlet of the pressure control valve is not vaporized.

Method of simulating the absorption of plane waves using FEM software tools

A novel and useful method of visualization by detection of EM radiation being irradiated or reflected from objects in the imager's field of view using Finite Element Method (FEM) simulation software tools. The methodology provides a verification method of antenna operation from an electrical point of view since bolometer performance cannot be estimated using regular antenna parameters such as directivity, gain, impedance matching, etc. as the bolometer does not behave as an antenna but rather behaves as an absorber. An incident wave is triggered on the absorber and the absorption of the bolometer structure is estimated using commercially available Finite Element Method (FEM) software (e.g., ANSYS® HFSS software, CST MICROWAVE STUDIO®, etc.). How much of the energy is reflected is subsequently measured. The energy which is not reflected is considered to be absorbed by the absorber.

Method of simulating the absorption of plane waves using FEM software tools

A novel and useful method of visualization by detection of EM radiation being irradiated or reflected from objects in the imager's field of view using Finite Element Method (FEM) simulation software tools. The methodology provides a verification method of antenna operation from an electrical point of view since bolometer performance cannot be estimated using regular antenna parameters such as directivity, gain, impedance matching, etc. as the bolometer does not behave as an antenna but rather behaves as an absorber. An incident wave is triggered on the absorber and the absorption of the bolometer structure is estimated using commercially available Finite Element Method (FEM) software (e.g., ANSYS® HFSS software, CST MICROWAVE STUDIO®, etc.). How much of the energy is reflected is subsequently measured. The energy which is not reflected is considered to be absorbed by the absorber.

SEPARATION DEVICES, ASSOCIATED METHODS, AND SYSTEMS

A system for isolating a target molecule from a bioprocess fluid includes a single-use disposable separation device having a plurality of perimeter-bonded layers defining one or more mesofluidic channels of the separation device, wherein each layer includes a biocompatible polymer material, wherein the separation device is configured to separate at least a portion of particles from the bioprocess fluid to generate a substantially clarified bioprocess fluid, and a chromatography system fluidically coupled at the outflow of the separation device in a configuration for further processing the clarified bioprocess fluid.

SEPARATION DEVICES, ASSOCIATED METHODS, AND SYSTEMS

A system for isolating a target molecule from a bioprocess fluid includes a single-use disposable separation device having a plurality of perimeter-bonded layers defining one or more mesofluidic channels of the separation device, wherein each layer includes a biocompatible polymer material, wherein the separation device is configured to separate at least a portion of particles from the bioprocess fluid to generate a substantially clarified bioprocess fluid, and a chromatography system fluidically coupled at the outflow of the separation device in a configuration for further processing the clarified bioprocess fluid.

Systems and methods for analyzing odors

An odor analysis system is provided to analyze odors present at a particular location and perform a preliminary identification of the odors while still at the location. The odor analysis system can have an odor processing device that collects samples of the odors and provides a series of odor notes to a user. The odor notes can be based on the separated and concentrated molecules in the collected sample. The odor analysis system can also include a hand-held computing device with a user interface that permits the user to enter information, both verbally and through touch input, about the series of odor notes provided by the odor processing device. The information entered by the user about the series of odor notes along with retention index information about the series of odor notes can be to perform a preliminarily identification of the molecules associated with the odors present at the location.

METHOD AND CHROMATOGRAPHY SYSTEM FOR DETERMINING AMOUNT AND PURITY OF A MULTIMERIC PROTEIN

The invention relates to a chromatography system and method for assessing amount and/or purity of a multimeric protein in a sample, wherein the chromatography system comprises two different affinity chromatography matrices connected via a switch valve.

FIELD FLOW FRACTIONATION DEVICE

Field flow fractionation device includes a channel switching unit for switching the connection of a second carrier fluid supply unit to any one of the second inlet port of an upper separation cell, the first inlet port of a lower separation cell, or the second inlet port of a lower separation cell. Furthermore, the second carrier fluid supply unit is connected to the second inlet port of an upper separation cell during the process of focusing to generate flow of carrier fluid counter to the flow of carrier fluid from the first inlet port within the upper separation cell, whereas the second carrier fluid supply unit is connected to the first inlet port or the second inlet port of a lower separation cell after conclusion of focusing in the upper separation cell.

PLANAR SEPARATION COMPONENT FOR GAS CHROMATOGRAPHY AND MANUFACTURING METHOD AND USE THEREOF

A planar separation component for gas chromatograph includes a substrate made of aluminum, a porous anodic aluminum oxide separation member, and a cover unit. The substrate has a planar body, and a first flow channel having a first inlet and a first outlet. The separation member is formed on the substrate, and has a channel-defining wall defining the first flow channel and a plurality of nanosized pores in spatial communication with the first flow channel. The cover unit is bonded to the planar body for covering the first flow channel. Methods for manufacturing the planar separation component and separating a mixture containing compounds different in boiling point using the planar separation component are also disclosed.