The present invention provides a detecting apparatus, including a storage chamber containing a treating fluid; wherein, the detecting apparatus is internally provided with a sharp-pointed portion; the storage chamber may make a movement relative to the sharp-pointed portion; the storage chamber will be pierced by the sharp-pointed portion during the moving process, such that the treating fluid in the storage chamber is released. The detecting apparatus further includes a collecting chamber; the released treating fluid may flow into the collecting chamber; the collecting chamber is disposed inside a first shell and used to contain a sample; an opening is disposed at an upper position of the first shell; the collecting chamber is internally provided with a testing element for detecting an analyte; the testing element is disposed on a carrier, and the carrier has a specific matching form with the collecting chamber. A buffer solution is disposed in an independent chamber of the detecting apparatus, and may be obtained at any time in need of detection and thus, is easy to be used. The carrier has a specific matching form with the collecting chamber in the first shell, such that the carrier has a definite and unique directional position after being inserted into the collecting chamber.

The present invention relates to an immunochromatographic assay device, comprising: a cover plate; an immunochromatographic assay kit; and a sample loading pad. A wet zone is defined by the cover plate and at least part of a sample loading portion of the sample loading pad disposed close to an installation position of the immunochromatographic assay kit. The height of the wet zone satisfies the following condition: when flowing into the wet zone, a sample solution is driven by capillary action to flow from a surface of the sample loading portion toward the immunochromatographic assay kit. A wet zone having a certain length is arranged in front of a sample loading zone of an immunochromatographic assay kit, such that when a sample solution flows into the wet zone, capillary action drives the sample solution to flow into the wet zone, thereby increasing a flow speed of the sample solution in the wet zone, allowing substantially simultaneous sample loading on immunochromatographic assay kits at different installation positions, and accordingly enhancing the consistency and uniformity of sample loading.

Temperature uniformity of a reaction liquid in a plurality of reaction containers of an automatic analysis device is maintained by a heat block. A strip-shaped heater heats the heat block, and is wound and attached on an outer circumference of the heat block so that both end regions of the strip-shaped heater are adjacent to each other. The strip-shaped heater includes a heat generating resistor that is heated by applying an electric current, an insulating film sandwiching the heat generating resistor, and first and second electrical feed lines that are attached to both end portions of the heat generating resistor and supply power to the heat generating resistor. The width of the heat generating resistor in both end regions of the strip-shaped heater is formed to be narrower than the width of the heat generating resistor in the other region thereof.

Automated liquid handling system for processing a plurality of samples in at least one microscope sample carrier, wherein the microscope sample carrier comprises a plurality of sample deposition wells, wherein each sample deposition well is defined on its lateral sides by one or more lateral walls and on its bottom side by a sample deposition surface, the automated liquid handling system comprising: a centrifuge adapted to centrifuge the microscope sample carrier; an automated transportation device adapted to transfer the plurality of samples and/or a plurality of liquids into and/or out of each of the plurality of sample deposition wells of the microscope sample carrier, and adapted for transporting the microscope sample carrier across the automated liquid handling system, wherein the automated transportation device is configured to couple with a coupling section of the microscope sample carrier; one or more storage containers for receiving and/or storing the plurality of samples and/or the plurality of liquids.

A microfluidic device includes a substrate having a first fluid inlet/outlet system, a second fluid inlet/outlet system, and a fluidic network between the first fluid inlet/outlet system and the second fluid inlet/outlet system and in fluid communication with the first fluid inlet/outlet system and the second fluid inlet/outlet system. The fluidic network includes a microfluidic channel network that is in fluid communication with the first fluid inlet/outlet system and spaced from the second fluid inlet/outlet system, a nanofluidic channel network fluidly connecting the microfluidic channel network and the second fluid inlet/outlet system, and a plurality of pores in fluid communication with the microfluidic channel network and the nanofluidic channel network.

A sample carrier device including a single substrate, a penetration structure and a fixing structure is provided. The penetration structure is formed on a side of the substrate. The penetration structure has a fluid passage. The fixing structure is formed on a side of the penetration structure. The sample carrier device is divided into an end portion, an observation portion and an operation portion. The user can separate the observation portion from the end portion by operating the operation portion. After the observation portion is separated from the end portion, the user can inject the sample into the fluid passage through a port of the fluid passage exposed to the observation portion. Once the sample is carried by the fluid passage of the observation portion, the user can seal the port of the fluid passage and place the observation portion in an electron microscope device.

The storage system is intended to provide users a device, that may securely hold biological samples within a cell in a space saving storage assembly. It is further an aim of the storage system to enable easy retrieval of the biological samples through a simple two-step retrieval action of the cell. Furthermore, the system includes a compact storage assembly that comprises multiple cells and canisters stacked together having efficient structural components that are suited for a typical freezer tank for biological samples. Additionally, the storage system comprises a simple elevator system that enables easy and fast retrieval of a single canister and cell from a large group of canisters.

Embodiments of the present disclosure can include a method for convective intracellular delivery including providing cells and molecules to a microchannel having compressive surfaces, wherein the compressive surfaces define compression gaps having a height of from 20 and 80% of the average cell diameter, and a plurality of relaxation spaces disposed between the compressive surfaces, flowing the cell medium through the microchannel, wherein as the cell medium flows through the microchannel, the plurality of cells undergo a convective intracellular delivery process comprising: compressing the plurality of cells, wherein the compressing causes the plurality of cells to undergo a loss in intracellular volume V.sub.loss, and passing the plurality of cells to a first relaxation space, wherein the plurality of cells undergo a gain in volume V.sub.gain and absorb a portion of the plurality of molecules.

A sampling device having a lower portion with a sample container. A cap is moveably attached with the lower portion and includes a cutting edge configured for cutting a leaf. When the cap is attached to the lower portion with a leaf there between, a leaf sample is deposited into the sample container of the lower portion. The cap includes a vent in fluid communication with the sample container such that the leaf sample is dried. A detachable label can extend from the lower portion.

A microfluidic device for image multiplexing includes a base structure and a fluid well insert. The base structure comprises an optical window. The fluid well insert configured to be coupled to the base structure and to retain a microscope slide for mounting a biological sample within the microfluidic device. The fluid well insert is further configured to provide a fluid to the biological sample. A fluid well insert lid is coupled to the fluid well insert or the fluid well insert comprises a fluid well insert lid.