A gas supply device for operation in an incubator allowing treatment of a culture within a shaker flask with gas independently of the composition and humidity of the gas atmosphere within the incubator individually supplies each shaker flask of the incubator with gas using a gas supply clamp detachably connected to the closure cap of each flask. The gas supply clamp has at least two elastic clamping jaws and a web connecting the clamping jaws to one another. The clamping jaws exert a clamping force on the side wall of the closure cap. The clamp is held in place by the elastic clamping jaws. Above a sterile filter in the closure cap, an individual gas atmosphere for treatment of the culture in the shaker flask is produced in a recess of the web above a gas passage in the closure cap.

Described are methods and systems for enhanced dissociation of cells from a solid biological tissue sample. In some embodiments, a self-contained cartridge apparatus includes a first chamber for receiving the tissue sample, enables ultrasonic energy from a transducer assembly of a processing unit to dissociate cells from the sample in the first chamber, and collect viable cells of interest from an aqueous suspension in a second chamber fluidly connected to the first chamber via a channel. In some embodiments, to enhance dissociation of viable cells, a filter device includes a tubular body configured to be telescopically inserted into a container containing the tissue sample in an aqueous fluid. The filter device also includes a cell-filter mesh that covers a bottom opening of the tubular body and that is configured to compress the tissue sample to expel cells from the sample when the filter device is fully inserted into the container.

A method of producing a cell structure includes applying a magnetic field, in a container (40), to a plurality of culture carriers to arrange the culture carriers. The culture carriers include at least one of a carrier (10) and a cell holding carrier (30), the carrier (10) having a magnetic portion (12), formed only in a part of the carrier (10), and a cell holder (11). The method also includes culturing cells (20) held on the cell holder (11) while maintaining the culture carriers in the arranged state.

Systems and methods for automated cell culturing are disclosed. In some embodiments, one or more cell culture vessels are fluidly connected with one or more multiport valves and one or more fluid pumps. The fluid pumps may pump various fluids into and out of the cell culture vessels as necessary to support cell growth, routed by the one or more multiport valves. In some embodiments, one or more components may be removable from other components so that some components may be prepared and sterilized independently prior to usage.

A mixing apparatus, comprising a drive unit (1) with a drive (10) and a shaft (11) which is pivotable about a pivot axis (A) and which is operatively connected to the drive (10), a pivot receptacle (2) which is arranged on the shaft (11), wherein the pivot axis (A) is substantially horizontally aligned, wherein the pivot receptacle (2) comprises a base (20) on which receptacles (21, 22) are provided which extend away from the base (20) and into which holders (3) for containers (7) are insertable.

A device for storing, incubating or manipulating biological samples, in particular incubating device or shaking device, comprising a sample chamber, an irradiation chamber, and a holder with a UV light source, wherein a sidewall of the irradiation chamber comprises a first mounting member and wherein the holder comprises a second mounting member configured to interact with the first mounting member for pre-mounting the holder to the sidewall.

An aggregated cell mass dispersing device (100) of the present invention includes: a storage container (101) storing a liquid (L) containing an aggregated cell mass; a pipette (102) whose tip is pushed against an inner bottom surface (101a) of the storage container; and an elastic body (103) supporting an outer bottom surface of the storage container.

The invention discloses an accurate positioning mechanism of a high-speed biological shaking table, which is characterized by comprising a servo motor output end, an eccentric shaft, a motor connecting disc, a positioning balancing weight, a positioning magnet and a Hall sensor, an eccentric shaft is installed at the top main body end of the servo motor, a motor connecting disc is installed on the surface of the eccentric shaft, a positioning balancing weight is arranged at the top end of the eccentric shaft, a positioning magnet is arranged on the surface of the side, away from the eccentric shaft, of the positioning balancing weight, and a Hall sensor is installed on the surface of the rocking shaft upper plate.

A clamping platform for a mechanical shaker, which allows automated release and fastening of microtiter plates that are subject to tolerances, includes at least two mounts arranged pairwise for the releasable fastening of the microtiter plates. The platform includes clamping jaws, on which a compression spring acts, actuatable with a link control having a linear drive. In conjunction with the compression spring, the geometry of the guide links allows compensation for the dimensional tolerances of the microtiter plates that are to be fixed by clamping. The spring force of the compression spring is determined such that the clamping jaws that are loaded by the compression spring exert the required clamping force in the deployed position onto the microtiter plates to be fixed.

The insert shelf (1) is characterized in that it has at least one means (3) with which an incubation medium located in an incubation vessel placed on the insert shelf (1) can be set in motion during an incubation treatment or during an incubation process in an incubator (2). For this purpose, the at least one means (3) can be operated electrically and/or preferably moved mechanically.