An embodiment of the claimed invention is directed to a method that greatly streamlines and reduces costs for tissue preparation, preservation, long-term storage and sample retrieval for molecular analysis using a method based on dried blood spot (DBS) technology. In this method, a small needle punch sample of freshly excised tissue will be homogenized in stabilizing reagent and inserted into a device containing absorbent material and drying agent. This device is suitable for long-term sample storage at ambient temperature and allows for easy removal of sections for biomarker analysis.

A telescoping electric pipette controller has a handle, a head end portion, an outer shell and a manual retainer. One end of the head end portion is arranged in an end portion of the handle in a penetrating manner, the outer shell is sheathed over an outer surface of the end portion of the handle, and one end portion of the manual retainer is rotatably connected to the outer shell. By means of opening or fastening the manual retainer, one end portion of the manual retainer is released outwards or pressed inwards against the head end portion, allowing extension and retraction of the head end portion relative to the handle. The extension and retraction, as well as the locking of part of a grip structure, are controlled by means of a switch, allowing the grip to change the length within a specific range.

The present invention defines a positioning assembly including a base part (110) and a holder part (120) for holding a device, whereby the assembly further includes a motor (160) for driving a displacement mechanism (150) mounted to the base part. The base part and the holder part are arranged parallel to each other and are connected via a displaceable slide link (140), which is configured to slide on a first guide rail (111) provided on the base part and on a second guide rail (122) provided on the holder part, whereby each guide rail extends in longitudinal direction (z). The slide link (140) is coupled to the displacement mechanism (150), which causes displacement of the slide link relative to the base part in longitudinal direction. Furthermore, the holder part (120) is moveably coupled to the base part (110) via a coupling arrangement which has a first element (115) provided on the base part, a second element (125) provided on the holder part and a third element provided on the slide link (140). The first, second and third elements of the coupling arrangement are configured to engage with each other such that linear displacement of the slide link (140) relative to the base part (110) in one direction causes linear displacement of the holder part (120) relative to the slide link in the same linear direction.

A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.

A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.

The invention relates to a pipetting device for receiving and dispensing fluid volumes. The pipetting device has a drive device with an electric motor and a gear device with a first output device. The gear device is driven by the electric motor by means of a rotary motion and is designed to transmit a rotary motion of the electric motor to the first output device. According to the invention, the gear device has a second output device and is designed to transmit a rotary motion of the electric motor to the second output device.

A pipette holder that includes: (i) a base; (ii) a recess made in the base, which can removably house a well support; (iii) a pipette support comprising a first housing into which can be inserted a pipette equipped with one or more tubular pipette cones that each comprise a tip intended for pipetting liquid, the first housing opening out onto the recess of the base, the pipette support being translationally mobile relative to the base in a direction parallel to an axis of the pipette cones and mobile between a first position in which the tip of each pipette cone is inserted in a well of the well support and at least one second position in which the tip is outside the well; and (iv) a second housing which can removably house a magnetized part.

A displacement device for displacing a displacement volume is disclosed. The device has a first fluid space and a second fluid space. A first piston is arranged in a movable manner within the first fluid space. The first fluid space is connectable to a pipetting device. The first piston is actuatable by an actuation volume of air or of liquid provided by the pipetting device. A second piston is arranged in a movable manner within the second fluid space. The second piston is constructed to displace a displacement volume of a fluid located within the second fluid space when the second piston is actuated. The second piston is actuated in dependence on the first piston that is actuated by the actuation volume. The actuation volume is different from the displacement volume, and a pipetting system has a displacement device and a method of displacing a displacement volume.

A bodily-fluid transfer device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.

A syringe-based device includes a housing, a pre-sample reservoir, and an actuator. The housing defines an inner volume between a substantially open proximal end portion and a distal end portion that includes a port couplable to a lumen-defining device. The pre-sample reservoir is fluidically couplable to the port to receive and isolate a first volume of bodily fluid. The actuator is at least partially disposed in the inner volume and has a proximal end portion that includes an engagement portion and a distal end portion that includes a sealing member. The engagement portion is configured to allow a user to selectively move the actuator between a first configuration such that bodily fluid can flow from the port to the pre-sample reservoir, and a second configuration such that bodily fluid can flow from the port to a sample reservoir defined at least in part by the sealing member and the housing.