A tissue processing system for processing a laboratory slide includes a slide holder for holding the slide, an outlet port positioned to direct a fluid stream onto the slide, and a device for moving the slide holder relative to the outlet port, or vice versa, to adjust a point on the slide at which the fluid stream is delivered onto the laboratory slide. The slide holder includes an absorbent pad configured to be positioned between one wall of the plurality of walls and a free edge of the slide for absorbing fluid travelling along the slide. A manifold of the system includes a first outlet port that directs a first fluid stream from a first fluid passageway onto the slide, and a second outlet port that directs a second fluid stream from a second fluid passageway onto a location of the slide that differs from the first fluid stream.

An apparatus and method for lyophilization, the apparatus includes a block made from a conductive material. The block has multiple wells dimensioned to receive containers wherein the depth of the wells is proportional to the length of the containers. A silicone pad covers the well and can secure the containers in the well. A metal plate can secure the silicone pad by fastening it to the block. The silicone plate and the metal plate can have vents to allow vapors from the containers to escape. The apparatus can be turned up to 90 degrees resulting in the turning of the containers from an upright position to a horizontal position. The container can be a syringe.

A perfusion manifold assembly is described that allows for perfusion of a microfluidic device, such as an organ on a chip microfluidic device comprising cells that mimic cells in an organ in the body, that is detachably linked with said assembly so that fluid enters ports of the microfluidic device from a fluid reservoir, optionally without tubing, at a controllable flow rate.

A culture module is contemplated that allows the perfusion and optionally mechanical actuation of one or more microfluidic devices, such as organ-on-a-chip microfluidic devices comprising cells that mimic at least one function of an organ in the body.

Systems for operating a microfluidic device are described. The systems comprise a first surface configured to interface and operatively couple with a microfluidic device and a lid configured to retain the microfluidic device on the first surface. The lid comprises a first portion having a first fluid port configured to operatively couple with and flow fluidic medium into and/or out of a first fluid inlet/outlet of the microfluidic device and a second portion having a second fluid port configured to operatively couple with and flow fluidic medium into and/or out of a second fluid inlet/outlet of the microfluidic device. The second portion of the lid is separable from the first portion and movable between a closed position in which the second fluid port of the second portion of the cover is operatively coupled with the second fluid inlet/outlet of the microfluidic device and an open position in which a portion of the microfluidic device that contains the second fluid inlet/outlet is exposed. Other embodiments are described.

An integrated pathology system includes a tissue embedding module configured to embed a tissue sample into an embedding material to prepare a tissue block, a sectioning and slide creating module configured to remove one or more tissue sections from the tissue block and place the one or more tissue sections onto one or more slides, a staining module configured to stain the one or more tissue sections on the slides, and a cover-slipper module configured to place a cover onto the one or more stained tissue sections. The system further includes one or more transfer devices configured to integrate the modules and a processor in communication with the modules for controlling one or more processes performed by the modules and the one or more transfer devices for controlling the integration of the modules.

An air-drying storage device for cleaned slides, including a storage box and a slide rack; an upper right corner in the storage box is fixedly provided with a miniature air intaking pump, a lower left corner in the storage box is fixedly provided with a miniature air expelling pump; a plurality of positioning plates are arranged on left and right inner walls of the storage box; the slide rack is detachably arranged between the positioning plates; an upper end of the storage box is provided with an electric control box configured to controls entire circuit. The air expelling pump and the air expelling pump accelerate the air flow rate inside the storage box; a sealing device and a magnetic device are arranged between edges of the box doors and edges of the storage box to prevent air leakage; an ultraviolet sterilization lamp sterilize the inside of the storage box.

A method for performing a magnetic separation procedure that includes transporting a receptacle containing a fluid medium to a first location of a system, where the fluid medium contains both a sample material and a suspension of magnetically-responsive solid supports. At the first location, the fluid medium is exposed to a first magnetic field for a first dwell period, thereby isolating the solid supports within the receptacle, where no portion of the fluid medium is removed from the receptacle at the first location. The receptacle is then transported from the first location to a second location of the system, where the fluid medium is exposed to a second magnetic field for a second dwell period. Following the second dwell period, at least a portion of the fluid medium is removed from the receptacle. A suspension fluid is then dispensed into the receptacle, and the contents of the receptacle are agitated to suspend the solid supports within the suspension fluid.

Disclosed are methods for isolating polymerase complexes from a mixture of polymerase complex components. The polymerase complexes can comprise a nanopore to provide isolated nanopore sequencing complexes. The methods relate to the positive and negative isolation of the polymerase complexes and/or nanopore sequencing complexes. Also disclosed is a nucleic acid adaptor for isolating active polymerase complexes, polymerase complexes comprising the nucleic acid adaptor, and methods for isolating active polymerase complexes using the nucleic acid adaptor.

Active surface devices for and methods of providing dried reagents in microfluidic applications is disclosed. In one example, the active surface devices include one or more dried reagent spots in relation to an active surface in the reaction (or assay) chamber thereof. In another example, the active surface devices include a dried reagent coating on the surfaces of the reaction (or assay) chamber including the active surface. In one example, the presently disclosed active surface devices are micropost-based active surface devices for providing active mixing therein. Further, a method of forming a dried reagent spot in the active surface devices is provided. Further, a method of forming a dried reagent coating in the active surface devices is provided. Further, a method of using the active surface devices for providing dried reagents in microfluidic applications is provided.

A tiltable stage assembly includes a base and a tiltable stage operably coupled to the base and pivotable relative to the base. The tiltable stage is moveable between an initial position and a tilted position, wherein the tiltable stage is parallel with the base in the initial position and is oriented at an angle to the base when in the tilted position. The tiltable stage is biased to the initial position.