Apparatuses and methods for generating trace vapors are provided. The apparatus includes a controller and an oven. The controller includes: a processor, a memory storing at least one control program, a clean solution supply port constructed to output a clean solution, an analyte solution supply port constructed to output an analyte solution, a carrier gas inlet port constructed to receive a carrier gas, and a plurality of carrier gas supply controllers constructed to output the carrier gas. The oven includes a clean manifold, an analyte manifold, a clean solution nebulizer constructed to: receive the clean solution from the clean solution supply port, and the carrier gas from one of the plurality of carrier gas supply controllers, and output a clean solution vapor stream comprising the clean solution and the carrier gas to the clean manifold, an analyte solution nebulizer constructed to: receive the analyte solution from the analyte solution supply port and the carrier gas from another one of the plurality of carrier gas supply controllers, and output an analyte solution vapor stream comprising the analyte solution and the carrier gas to the analyte manifold, a pneumatic valve controllably connected to the processor and communicatively connected to the clean manifold and the analyte manifold, and an output supply port communicatively connected to the pneumatic valve. The controller is configured to operate the pneumatic valve to allow the clean vapor solution or the analyte vapor solution to enter the chamber and be provided to the output supply port.

Technologies for rapid equilibration for water isotope analysis are disclosed. In at least one illustrative embodiment, a vaporizer may include an injection block that defines a chamber and a septum positioned over an inlet of the chamber to seal the chamber. The chamber may be configured to be fluidly coupled to a pump to develop a vacuum within the chamber, and the septum may be configured to receive a needle that is inserted into the chamber. A thermally conductive wool may be positioned within the chamber and may be configured to receive a tip of the needle.

The disclosure relates to devices, solutions and methods for collecting and processing samples of bodily fluids containing cells (as well as embodiments for the collection, and processing and/or analysis of other fluids including toxic and/or hazardous substances/fluids). In addition, the disclosure relates generally to function genomic studies and to the isolation and preservation of cells from saliva and other bodily fluids (e.g., urine), for cellular analysis. With respect to devices for collection of bodily fluids, some embodiments include two mating bodies, a cap and a tube (for example), where, in some embodiments, the cap includes a closed interior space for holding a sample preservative solution and mates with the tube to constitute the (closed) sample collection device. Upon mating, the preservation solution flows into the closed interior space to preserve cells in the bodily fluid. The tube is configured to receive a donor sample of bodily fluid (e.g., saliva, urine), which can then be subjected to processing to extract a plurality of cells. The plurality of cells can be further processed to isolate one and/or another cell type therefrom. The plurality of cells, as well as the isolated cell type(s), can be analyzed for functional genomic and epigenetic studies, as well as biomarker discovery.

A wafer for carrying a biological sample includes a pair of circular discs, at least one of the discs being transparent. The wafer also includes a gap between the discs adapted to receive a biological sample. The compact circular shape of the wafer makes it particularly suited for use in a portable device in which the wafer is rotated to enable a camera to image different areas of the sample between the discs. The gap may be sized to pull a biological sample into the gap by capillary action.

A pathological specimen preparation device includes a stage portion including a stage, a reagent supply portion 150 capable of supplying a reagent to a substrate W mounted on the stage, a washing portion capable of supplying a washing solution to the substrate, an electric field stirring portion capable of stirring the reagent or the washing solution supplied to the substrate by applying an electric field to the reagent or the washing solution, and a control unit, wherein the washing portion, the reagent supply portion, and the electric field stirring portion are sequentially disposed in a Y direction as a first direction, and the device includes a stage transport mechanism that moves the stage in the Y direction, and a stage tilting mechanism that tilts the stage in an X direction as a second direction crossing the Y direction when the stage is positioned in the washing portion.

A thermal desorber assembly includes a housing and a desorption heater element mounted in the housing with a sample cavity defined between the desorption heater element and an inner wall of the housing. An outlet port is defined in the housing. A flow channel connects the sample cavity in fluid communication with the outlet port for conveying analytes from the sample cavity to the outlet port for introducing the analytes to a spectrometer.

An apparatus for measuring contaminants on a surface of a component is provided. An extraction vessel for holding a measurement fluid has an opening adapted to form a meniscus using the measurement fluid. An actuator moves at least one of the extraction vessel and the component to a position where the meniscus is in contact with the surface of the component. A transducer is positioned to provide acoustic energy to the measurement fluid.

A thermal desorber assembly includes a housing and a desorption heater element mounted in the housing with a sample cavity defined between the desorption heater element and an inner wall of the housing. An outlet port is defined in the housing. A flow channel connects the sample cavity in fluid communication with the outlet port for conveying analytes from the sample cavity to the outlet port for introducing the analytes to a spectrometer.

Methods and compositions for creating a de novo filtration structure for filtering, e.g., chemical, biological, or other samples prior to further manipulation of the samples are disclosed.

The other end of an individual sample supply channel one end of which is connected to a gas buffer container the inside of which is empty is connected to one sub-port of a valve that selects one of standard samples to be supplied to an ESI probe. During analysis, the standard sample stored in one of liquid sample containers is selected by switching a connection state of the valve. The standard sample supplied by being pushed by a gas sent to the liquid sample containers through liquid supply gas branch channels is sent to the ESI probe through a sample supply main channel. At the time of finishing analysis, when the valve is switched such that the sub-port and a main port are communicatively connected, a nitrogen gas is sent to the sample supply main channel, and the remaining liquid is discharged.