A composition for urine glucose detection includes a fixing agent, an indicator and glucose oxidase, wherein the fixing agent includes one or more selected from the group consisting of a soap base, gelatin, and natural fatty acids.

The present invention relates to a flow-through device comprising at least one separation column wherein a first packing component, which comprises particles of alumina and/or silica, and a second packing component, which comprises a powder of one or more hygroscopic salts are provided. The two packing components may be blended or layered in the device, which may comprise a single tube or a plurality of tubes arranged in a plate format, such as the wells of a multiwall plate or tubes in a rack. In addition, the invention relates to a method for removing one or more matrix components, such as pigments, from a biological sample, by passing said sample across a first packing component, which comprises particles of alumina and/or silica, and a second packing component, which comprises a powder of one or more hygroscopic salts.

This device comprises: a casing with an upper surface including a sample-dripping portion receiving a liquid sample containing nucleic acid and being dripped from a nozzle; a reaction tube: outwardly projecting from an end of the casing; including a storage space therein; and being formed so as to be installed within a measurement apparatus; a filter carrying the nucleic acid contained in the liquid sample; a filter-supporting body stored within the casing to support the filter in a manner such that the filter is capable of taking: a contacting position wherein the filter contacts with the liquid sample right below the sample-dripping portion; and a reaction position wherein the filter is positioned within the storage space of the reaction tube; and absorbing material capable of taking: a press-attaching position wherein the absorbing material is press-attached to the filter in the contacting position so that the filter absorbs the liquid sample contacting therewith; and a separating position wherein the absorbing material is removed from the press-attaching position so that the filter is allowed to freely move.

In an embodiment, the present disclosure pertains to a method of performing circulating tumor cell (CTC) analysis. In general, the method includes flowing a sample through a CTC microfluidic platform, deforming a CTC within the sample, measuring CTC deformation through an imprint of the deformed CTC, processing data related to the measuring, and at least one of identifying or characterizing parameters related to the data that enables at least one of detection of CTCs, enumeration of CTCs in the sample, characterization of biophysical properties, CTC cell size, CTC cell membrane deformability, stresses on CTC cell membranes, adhesion stress on CTC cells, normal stress of CTC cells, or combinations thereof. In some embodiments, the flowing includes passing the sample through at least one channel of the CTC microfluidic platform having a constricted section.

A test strip holder includes: a holding member at which at least a portion of a lower side of an inner periphery is a cylindrical surface having a cylindrical shape, and at whose interior a test strip is held, and at which a direction of an imaginary central axis of the cylindrical surface is a horizontal direction or a direction inclined with respect to a vertical direction; an opening portion provided in an outer surface of the holding member; a sorting member rotating at an interior of the holding member around a rotation axis that coincides with the central axis; a pushing piece projecting out from a distal end edge, which is parallel to the central axis, at the sorting member in a direction of rotation of the sorting member; and a sorting piece projecting out from a distal end of the pushing piece toward the cylindrical surface.

Implementations of a method for seeding sequence libraries on a surface of a sequencing flow cell that allow for spatial segregation of the libraries on the surface are provided. The spatial segregation can be used to index sequence reads from individual sequencing libraries to increase efficiency of subsequent data analysis. In some examples, hydrogel beads containing encapsulated sequencing libraries are captured on a sequencing flow cell and degraded in the presence of a liquid diffusion barrier to allow for the spatial segregation and seeding of the sequencing libraries on the surface of the flow cell. Additionally, examples of systems, methods and compositions are provided relating to flow cell devices configured for nucleic acid library preparation and single cell sequencing. Some examples include flow cell devices having a hydrogel with genetic material disposed therein, and which is retained within the hydrogel during nucleic acid processing.

Apparatus and method for removing liquid from exterior surfaces of sample wells in a well plate. Wells that have water or other liquid on an exterior surface, e.g., after acoustic energy treatment in a water bath, may have the liquid removed by contacting the exterior surfaces of the sample wells with an absorbent material. A pad made of absorbent material may have a plurality of openings arranged to receive an array of sample wells inserted into the openings so that liquid can be removed from each of the sample wells.

A passive sampling device is provided that is comprised of a member having a first surface and a second surface opposite the first surface and a hole through the member extending from the first surface to the second surface. An adsorbent material is positioned between two mesh members. The adsorbent material allows for efficient and selective removal of organic molecules, such as, for example, perfluoroalkyl substances.

A microfluidic preconcentrator is provided, designed to receive a gas sample containing gaseous pollutants such as volatile organic compounds, to concentrate the gaseous pollutants and to transfer them to an analysis device. An assembly comprising an enclosure, a microfluidic preconcentrator, connectors and a means for holding the microfluidic preconcentrator inside the enclosure, a heating device and a cooling device, are provided.

A portable device (1) for detecting and quantifying a concentration of a marker, for example TROPONIN I, present in a sample of biological fluid. The device (1) comprises a cartridge (100) adapted to receive the biological fluid sample and comprising at least one reactive agent configured to bind to the marker defining an electrochemiluminescent solution. The cartridge (100) is coupled to an electrode cell (101) configured to supply electrical energy to the electrochemiluminescent solution so as to trigger an electrochemiluminescence reaction of the electrochemiluminescent solution, generating a light signal representative of a concentration value of the marker in the biological fluid sample. The device (1) further comprises an analyzer (200), connectable to the cartridge (100) and configured to receive and analyze at least one property of the light signal so as to quantify a concentration of the marker in the biological fluid.