The present invention relates to a device and a method for evaluating performance of a deodorant using a superabsorbent polymer (SAP), and the device and method are capable of quantitatively evaluating deodorant performance by collecting ammonia adsorbed to deodorant materials including the SAP and measuring the amount of ammonia thereof.

The present invention relates to a device and a method for evaluating performance of a deodorant using a superabsorbent polymer (SAP), and the device and method are capable of quantitatively evaluating deodorant performance by collecting ammonia adsorbed to deodorant materials including the SAP and measuring the amount of ammonia thereof.

A method of cleaning a detection cell of an electron capture detector in which the detection cell includes a radiation source that emits radiation, a sample gas introduction port through which a sample gas is introduced, and a collector electrode, includes: introducing a cleaning gas into the detection cell of the electron capture detector.

Methods, devices, systems, and apparatuses are provided for the image analysis of measurement of biological samples.

The invention generally relates to detecting biological substances. In certain aspects, the invention is directed to a method directing one or more wavelengths of light within a deep ultraviolet (UV) spectrum into a medium to excite a biological substance in the medium, detect emission from the excited biological substance via a plurality of semiconductor photodetectors, and analyze the deep UV emission data for presence of a deep UV spectral signature indicative of the biological substance, wherein presence of the deep UV spectral signature indicates that the medium comprises a biological substance. The invention is also directed to identifying a pathogen in a medium comprising a pathogen and a non-pathogen biological substance.

A fluidic coupler to engage a plurality of flow cells of a sensor device includes a body and a plurality of fluidics interfaces formed in the body. Each fluidic interface of the plurality of fluidics interfaces includes an opening, a first port in fluid communication with the opening, a second port, and a third port in fluidic communication with the second port.

The present disclosure provides devices, systems, kits and methods useful for quantitation of biomolecules such as intact proteins and nucleic acids.

A molecular detection apparatus according to a embodiment includes: a collection unit which collects detection target gases each containing molecule to be detected; a concentration adjusting unit which dilutes and/or concentrates the molecule, and generates a plurality of detection target gases having different concentrations of the molecule; a detection unit to which the plurality of detection target gases are sequentially introduced, and which includes a plurality of detection cells each outputting detection signals based on the concentrations of the molecule in the plurality of detection target gases; and a discrimination unit which discriminates the molecule by change tendencies of the detection signals based on the concentrations of the molecule.

A molecular detection apparatus according to a embodiment includes: a collection unit which collects detection target gases each containing molecule to be detected; a concentration adjusting unit which dilutes and/or concentrates the molecule, and generates a plurality of detection target gases having different concentrations of the molecule; a detection unit to which the plurality of detection target gases are sequentially introduced, and which includes a plurality of detection cells each outputting detection signals based on the concentrations of the molecule in the plurality of detection target gases; and a discrimination unit which discriminates the molecule by change tendencies of the detection signals based on the concentrations of the molecule.

An embodiment of a system includes a compartment-generating device, a compartment detector, and electronic computing circuitry. The device is configured to generate compartments of a digital assay, at least one of the compartments having a respective volume that is different from a respective volume of each of at least another one of the compartments. The detector is configured to determine a number of the compartments each having a respective number of a target that is greater than a threshold number of the target. And the electronic circuitry is configured to determine a bulk concentration of the target in a source of the sample in response to the determined number of compartments. Because such a system can be configured to estimate a bulk concentration of a target in a source from a polydisperse digital assay, the system can be portable, and lower-cost and faster, than conventional systems.