A container for storing a histological sample comprises a container housing having an open top end and a bottom end defining a container interior. The container interior is configured to hold a fluid and receive the sample. A removable lid encloses the open top end. A container insert engages the container housing so as to substantially inhibit leaking of the fluid from the container. The insert includes an aperture configured to permit a sample holder containing the sample passage therethrough so as to enable depositing of the sample within the fluid in the container.

The present disclosure relates to devices, systems, and methods for modeling ocular translaminar pressure gradients ex vivo. A first fluid pressure level can be applied to a first side of a wall of donor eye cup (e.g., a posterior human eye cup) to simulate intracranial pressure (ICP), for example around the optical nerve head (ONH), and a second fluid pressure level can be applied to a second side of the wall of the donor eye cup to simulate intraocular pressure (IOP). These devices, systems, and methods are unique in that they allow ex vivo modeling of dynamic changes in translaminar pressure gradients.

The present invention is directed to a cap for a biochip storage well. The cap comprises a resilient sealant layer capable, under the application of pressure, of forming a vapour-proof seal with a line contact interface formation extending around the perimeter of a biochip storage well.

An assay assembly comprising the cap of the invention and a biochip storage is disclosed. Methods of sealing a biochip storage well using a cap of the invention are also disclosed.

To provide an electric measuring cartridge capable of decreasing a risk of contact with a connecting unit. Provided is an electric measuring cartridge at least provided with a biological sample holding unit which accommodates a biological sample, at least a pair of electrodes fixed to the biological sample holding unit, a connecting unit which electrically connects the electrodes to an external circuit, and a protecting unit which protects the connecting unit.

Disclosed herein are evacuated blood collection tubes comprising protease inhibitor cocktails in liquid form and uses thereof for assessing features associated with the contact system in a subject, including the endogenous level of contact system activation, the endogenous level of a drug that targets a component of contact system during treatment, and/or the immunogenicity of such a drug.

Apparatus is provided for testing a biological fluid for presence of a biological particulate. The apparatus includes a tube, a plunger sized and shaped to be inserted into and advanced within the tube, and a filter. The apparatus is configured such that as the plunger is advanced within the tube while the biological fluid is within the tube, the biological fluid in the tube is pushed through the filter, thereby trapping, by the filter, the biological particulate present in the biological fluid. The apparatus is shaped so as to define at least one enclosed cavity containing a biological particulate-presence-testing-facilitation solution configured to test for the presence of the biological particulate trapped by the filter. The enclosed cavity is configured to open while the plunger is inside the tube, so as to release the biological particulate-presence-testing-facilitation solution within the tube. Other embodiments are also described.

A separation container for extracting a portion of a sample for use or testing and method for preparing samples for downstream use or testing are provided. The separation container may include a body defining an internal chamber. The body may define an opening, and the body may be configured to receive the sample within the internal chamber. The separation container may further include a seal disposed across the opening, such that the seal may be configured to seal the opening of the body, and a plunger movably disposed at least partially inside the internal chamber. The plunger may be configured to be actuated to open the seal and express the portion of the sample.

Systems and methods are provided for analyzing a test sample is provided. A system includes an outer container having first and second ends and a base affixed to the first end. The system includes a motorized mixer affixed to the base. The system includes an inner container having first and second ends. The inner container is sized to be received within the outer container. The first end of the inner container has a membrane layer that is pierceable by the mixer when the inner container is received by the outer container to bring the mixer into contact with a test sample in the inner container. The system further includes a test sensor configured for contact with the test sample, and one or more processors for receiving signals from the test sensor following actuation of the mixer to cause mixing of the sample and analyzing the sample based on the signals.

A device for storage and transportation of an empty case of a firearm bullet cartridge for forensic investigation, wherein said case comprises a cylindrical shell which is substantially closed at one end, said device comprising a container having a bottom wall, a side wall and an opening, and comprising a cap for sealing the opening of said container, wherein said cap is provided with holding means arranged to be inserted in the empty case for restricting lateral movement of the empty case in said container.

Disclosed is an analysis system for analyzing water and wastewater, comprising an analysis device that includes a device housing which accommodates device components and which has an inlet on a housing surface, said inlet being designed as an injection port through which a substance to be analyzed can be introduced into a device component when the device housing is closed, and comprising a syringe that includes an injection needle outlet, the surface normal of which is congruent with the longitudinal axis; and/or the syringe includes an automatic ejection element for ejecting a predetermined amount of substance within a predetermined injection period.