An air replenishing fume hood includes a cabinet, a door set, an air replenishing unit and an air guiding unit. The cabinet has an inner casing defining an operating chamber and having an air inlet and an air outlet. A side of the cabinet includes an operation window. A first air passage is formed between the inner casing and the cabinet. The door set includes an outer door leaf adapted to open or close the operation window, and an inner door leaf adapted to open or close the air inlet. An end of the air replenishing unit extends into an external space via an outdoor tube, and another end of the air replenishing unit is connected to the first air passage via an extension tube. The air guiding unit includes an end connected to the air outlet, and another end extending into the external space or a collection tank.

A reagent dispensing apparatus includes a housing having a cavity with an opening and an aperture; and a plunger that includes a first member, that fits through the aperture, that is associated with a first seal. The plunger includes a second member associated with the first seal and a second seal that together form a first chamber, within the cavity, in which a first reagent is stored. The plunger includes a safety mechanism that controls movement of the plunger within the cavity. The apparatus includes a frangible seal that covers the opening and together with the second seal forms a second chamber, within the cavity, that stores a second reagent. When the first end is depressed and the safety mechanism is disengaged, the frangible seal is breached causing the evacuation of the first reagent or the second reagent through the opening.

The purpose of the present invention is to provide a clean air device that can reduce the risk of contamination due to static electricity. Provided is a biosafety cabinet or a clean air device that connects a biosafety cabinet and a clean booth, wherein a static eliminator (ionizer) that generates a corona discharge by way of concentrating an electric field on a needle-shaped discharge electrode and eliminates static with ionized air is disposed directly above an air flow branching point where air supplied to a work space branches to the front face and to rear face inside the biosafety cabinet.

A digital slide scanning apparatus includes a safety light curtain that operates to disable the motor that rotates the carousel when the presence of an object (e.g., the fingers of an operator) is detected within a predetermined area of the carousel. The light curtain also operates to disable the motor that rotates the carousel when an improperly positioned glass slide or slide rack is detected. The digital slide scanning apparatus also includes a multi-color status indicator for each rack slot that indicates the rack slot location of an improperly positioned glass slide or slide rack.

A safety cabinet has an opening portion in the front surface of a work room and a front shutter and supplies clean air to the work room from above. A side slit is provided in the side surface of the work room, air from the provided side slit joins an air flow path suctioned from a front grille of a workbench forming the bottom surface of the work room, and the turbulence of an airstream can be prevented even when a device is installed in the work room.

A slide rack carousel is provided that includes a base that is configured to support a plurality of slide rack spacers that extend upward from an upper surface of the base. Adjacent slide rack spacers define a slide rack slot of a predetermined size. The plurality of slide rack spacers may include slide rack spacers of varying sizes and therefore a plurality slide rack slot sizes can be selectively configured on the carousel in accordance with the positioning and size of the plurality of slide rack spacers that are attached to the base of the carousel. Accordingly, a desired number of 13 slide rack slots and a desired number of 23 slide rack slots can be configured on the base of the slide rack carousel.

The disclosed devices, systems and methods related to the use of a test tube rack to assist with withdrawal of a needle from a container. The rack has a plurality of notches on a top shelf and corresponding openings on a second shelf that allow for the movement of a container stored therein between positions so as to prevent needle sticks and allow for one-handed operation.

Fluid containment pressure vessel that eliminates the outer support housing present in certain conventional vessels, and provides an improved cap-to-body interface. In certain embodiments, the cap is threaded and configured to threadingly engage with the body of the pressure vessel, and has sufficient structural integrity to withstand the pressures in the device without the need for a support housing. In certain embodiments, an interlock mechanism is provided that prevents the cap from being opened (e.g., removed from the body) while the device is under pressure. In certain embodiments, a pressure relief valve is provided with a pre-loaded biasing mechanism to achieve the required pressure release rate. The vessel can be used for sample preparation, including purification or concentration of samples, particularly protein samples.

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.

Fluid containment pressure vessel that eliminates the outer support housing present in certain conventional vessels, and provides an improved cap-to-body interface. In certain embodiments, the cap is threaded and configured to threadingly engage with the body of the pressure vessel, and has sufficient structural integrity to withstand the pressures in the device without the need for a support housing. In certain embodiments, an interlock mechanism is provided that prevents the cap from being opened (e.g., removed from the body) while the device is under pressure. In certain embodiments, a pressure relief valve is provided with a pre-loaded biasing mechanism to achieve the required pressure release rate. The vessel can be used for sample preparation, including purification or concentration of samples, particularly protein samples.