Disclosed herein are cell processing systems, devices, and methods thereof. A system for cell processing may comprise a plurality of instruments each independently configured to perform one or more cell processing operations upon a cartridge, and a robot capable of moving the cartridge between each of the plurality of instruments.

A system for processing biological material includes a first module and at least a second module, in which each of said first and second modules has at least the following identical characteristics: a size and a shape of a housing; a storage device being rotatably located within said housing; and a plurality of plate slots located in the storage device for receiving plates or containers carrying pipette tips, cell cultures or liquids. The first and second modules are selected from a process module, a storage module, an incubator, a freezer, a plastic-ware store, a refrigerator or a centrifuge.

One or more light sources may apply stimuli to a colony of organisms. The stimuli may include visible and non-visible light. The stimuli, taken together, may tend to favor survival of organisms that are adapted to perform photosynthesis which involves absorbing energy from infrared or ultraviolet light. In some cases, the set of stimuli may include illuminating the entire colony of organisms with green light, illuminating only a first portion of the colony with pulsed ultraviolet light, and illuminating only a second portion of the colony with pulsed infrared light.

The invention provides a device for growing cells—referred to as a cassette. The cell culturing device includes a housing that contains a lid having an optically clear window; a fluid distribution channel; a sample injection port fluidically connected to the fluid distribution channel; a base housing a porous media pad; and a media injection port fluidically connected to the media pad. The lid mates to the base to form a sterile seal; the fluid distribution channel is disposed over the media pad, which is viewable through the optical window; and sample fluid introduced into the fluid distribution channel is distributed evenly to the media pad, e.g., via a plurality of channels. The invention also provides kits that include cassettes of the invention and a tube set.

Disclosed herein are cell processing systems, devices, and methods thereof. A system for cell processing may comprise a plurality of instruments each independently configured to perform one or more cell processing operations upon a cartridge, and a robot capable of moving the cartridge between each of the plurality of instruments.

A cell culture tool configured to be produced in a simple facility to obtain a cell mass having a desired shape. The cell culture tool includes a cell culture base layer that contains a cell culture base. The cell culture base layer has a cell adhesive area to which a cell is adherable and a cell adhesion inhibitory area where cell adhesion is inhibited. The cell adhesion inhibitory area includes a modified product of the cell culture base.

A cell culture system or assembly, flask, plate and dish for growing, viewing and evaluating cells; and methods of use.

A columnar cell culture vessel is disclosed. The columnar cell culture vessel according to an embodiment of the present disclosure may include: a cylindrical body having a chamber disposed therein, an inlet disposed through one side in an axial direction, and an outlet disposed through in the axial direction; a first cap coupled to the inlet and having an inflow port disposed therethrough; a second cap coupled to the outlet and having a discharge port disposed therethrough; and a support which is filled in the chamber and to which cells are attached to be cultured, wherein a culture solution is introduced into the chamber through the inflow port and discharged to the outside of the chamber through the discharge port.

An apparatus includes a cellular culture container having an interior cavity. A cellular culture area is located in the interior cavity. The cellular culture area is configured to receive at least one cell to be cultured. A condensation director is configured to reduce and/or prevent the entry of condensation into the cellular culture area.

Massively parallel high throughput single-cell optoperation and their uses thereof are disclosed. The disclosed method teaches the use of parallel single-cell printing technique using SU-8 membrane and nanosecond pulsed laser to espouse on single-cell with micro-dish pattern structure. The platform is able to effectively deliver different (small to large) cargo in a different cell type with high transfection efficiency and high cell viability at parallel single-cell resolution. The proposed Bio-MEMS device has potential applications in personalized and regenerative medicine.