A laboratory weighing kit comprises two layers: a disposable paper-structured weighing boat in the upper layer and a corresponding-shaped weighing base in the lower layer. The weighing boat has a sample loading portion in the rear to carry chemicals or samples, and a funnel portion in the front to transfer samples. In order to consolidate storage space, either the front funnel can be opened to two portions or the back wall of the weighing boat is opened. The weighing boat can be creased to form a permanent fold. The weighing boat in the upper layer can be either removable from or permanently attached to the weighing base in the lower layer.

An storage container for a biological fluid includes, for example, a sequence of elongated compartments interconnected by passageways. The sequence forms a single continuous tube or ribbon having a first end, to which a first port is optionally connected, and a second end, to which a second port is also optionally connected. After filling the container with a biological fluid, multiples closures are formed across the single continuous tube or ribbon, for example across each passageway, to seal the compartments.

Pipetting containers, such as reservoirs, reservoir liners, microplates, PCR plates, microtubes and PCR tubes, include anti-vacuum channels on the bottom wall of the receptacle to prevent a pipette tip vacuum engaging the wall during aspiration. The groupings of anti-vacuum channels are located on the bottom surface facing upward into the basin that holds liquid samples or reagents. The anti-vacuum channels also lower the required working volume for pipetting and reduce liquid waste.

A reagent container is disclosed that is installed in an analyzer for use and stores a reagent supplied to the analyzer via an aspiration tube. The reagent container includes a container body. The container body includes a tubular member with an opening into which the aspiration tube is inserted from above, and a bag-shaped member joined to the tubular member and storing the reagent. The container body comprises a penetration prevention member that prevents a tip of the aspiration tube 90 inserted through the opening from penetrating the container body.

A method of preparing reagents includes inserting a cartridge into an instrument. The cartridge includes a plurality of reagent enclosures disposed in a cavity of the cartridge and exposing a port to an exterior of the cartridge. Each reagent enclosure includes a reagent container including a reagent and an internal cavity defining a compressible volume, an opening defined through the reagent container to the internal cavity. The method further includes connecting a plurality of fluid ports to the openings of the plurality of reagent enclosures; applying a solution through the fluid ports to at least partially fill the plurality of reagent enclosures; and cycling a pressure of the cavity, whereby for each of the reagent enclosures, during increasing pressure, the solution enters the internal cavity of the reagent container, combines with the reagent, and compresses the compressible volume, and during decreasing pressure, the compressible volume decreases and the reagent is ejected through the opening.

The present invention relates to a disposable container comprising a side wall, top and bottom, wherein the side wall and the bottom comprise a flexible material, wherein the side wall, top and bottom are joined together to define the container with an interior compartment for keeping a fluid inside the container. The bottom of the container comprises at least one portion of rigid or semi-rigid material comprising a folding means that enables folding of the bottom. Thus an easy way of folding the bottom of the container is provided.

Embodiments described herein relate to an apparatus for positioning and securing an excised biological tissue specimen for imaging and analysis. In some embodiments, an apparatus includes a sample bag defining an inner volume configured to receive a biological tissue sample, and a sealing member coupled to the sample bag. An imaging window is disposed and configured to be placed in contact with at least a portion of the biological tissue sample, and a positioning member is coupled to the imaging window and is configured to be disposed against the sealing member to substantially seal the inner volume. The positioning member includes a vacuum port disposed and configured to be aligned with a vacuum source to withdraw air from the inner volume of the sample bag.

A device for generating a droplet array, which comprises a substrate, a roller on the substrate, and a microgrooved chip on the outer surface of the roller, wherein a sealant is on a surface of the substrate close to the roller and the microgrooved chip comprises a chip body fitted to the roller and an array of microgrooves arranged on the chip body, the array of microgrooves consisting of a plurality of microgrooves arranged at intervals on the chip body. When the roller rolls, liquid between the substrate and the roller enters the microgrooves and forms droplets while the microgrooved chip detaches from the roller and combines with the sealant which seals the microgrooves, generating a droplet array. The device generates a droplet array having uniform droplet size, good repeatability. Further, the method is simple and highly efficient, and has broad application prospects in the fields of medicine and biology.

A method is provided for measuring parameters of state of a fluid contained in a container (10, 10′) that has a sensor carrier plate with plural sensors (S01-S10, S01′-S10′). Each sensor has a sensor head in operative contact with the interior of the container (10, 10′) and in operative contact with an external control unit (12). The external control unit (12) receives measurement data generated by the sensor heads of active sensors via their communication link and processes the data. An activation data record (24, 24′) is assigned to each sensor (S01-S10, S01′-S10′) and is recorded in a manner that is accessible for the external control unit (12). The external control unit (12) first accesses the activation data records (24, 24′), then classifies the sensors (S01-S10, S01′-S10′) as activatable or nonactivatable sensors, and subsequently activates only those sensors classified as activatable sensors.

A microbial detection device and methods of use are provided. The device comprises a water-proof pouch that includes a first wall portion, a second wall portion, and a porous membrane filter disposed in the pouch between the first and second wall portions. The filter membrane divides the pouch into first and second compartments. A dry, cold water-soluble gelling agent is adhered to the pouch in the first compartment and an absorbent pad is disposed in the second compartment. A release liner removably adhered to the first adhesive layer.