A method for producing H.sub.2, methane, VFAs and alcohols from organic material, including the steps of introducing organic material and microorganisms into a completely mixed bioreactor for producing H.sub.2, CO.sub.2, VFAs, and alcohols; recovering H2 and CO2; recovering a first liquid effluent including microorganisms, VFAs, and alcohols; introducing the first liquid effluent into a gravity settler for separating into a first biomass including microorganisms and a second liquid effluent including VFAs, alcohols and microorganisms; introducing the second liquid effluent into a separation module for separating into a second biomass including microorganisms and a third liquid effluent including VFAs and alcohols; recovering at least a portion of the third liquid effluent; and providing a recovered biomass by recovering at least a portion of the first biomass, the second biomass, or both, and introducing the recovered biomass into a biomethanator for production of CH.sub.4 and CO.sub.2.

The present invention relates to a pillar assembly and an apparatus for producing a sample block comprising the same, and according to one aspect of the present invention, it is possible to change arrangement of pillars, and sample slices can be easily obtained from the sample block.

A system and method for growing and maintaining biological material including producing a protein associated with the tissue, selecting cells associated with the tissue, expanding the cells, creating at least one tissue bio-ink including the expanded cells, printing the at least one tissue bio-ink in at least one tissue growth medium mixture, growing the tissue from the printed at least one tissue bio-ink, and maintaining viability of the tissue.

Metastable state spore incubation mixing systems are described. An example system includes a spore container to store spores, a nutrient container, an arrangement of valves and tubes, a reciprocating pump, a mixing tube, and a holding tank. In a drawing phase of the system, a controller can control the reciprocating pump to draw a ratioed volume of the spores, the nutrients, and water through the valves and tubes. During an expelling phase of the system, the controller can control flow control valves to direct the spores, nutrients, and water through the mixing tube and into the holding tank. The controller can also direct a heater to heat the mixture in the holding tank to a predetermined temperature. Once the mixture reaches the temperature, the controller can also direct the system through a number of other phases of operation, including cooling and purging phases.

The present invention relates to methods and devices for monitoring events occurred in a single cell or examining cell characteristics in a single cell in a massive parallel and real-time manner. In one embodiment, the present invention provides a single-cell culturing system for culturing and monitoring a large number of cells independently at single-cell level. In one embodiment, the present invention provides methods and devices for studying or monitoring single-cell response to an external stimulus in a massive parallel and real-time manner. In one embodiment, the present invention provides methods and devices for studying or monitoring drug response at single-cell level in a massive parallel and real-time manner.

Provided are a tumour immunogen, a preparation method therefore, and an application. After localised sequential cooling-heating treatment is performed on tumour tissue and/or cells, the tumour tissue and/or cells release a large amount of tumour immunogen heat shock protein 70. The obtained tumour immunogen can activate the body's tumour immune system, to convert immunosuppressive cells into mature dendritic cells, thereby increasing immunogen presentation, and activating tumour immunity.

An information processing apparatus includes an acquisition unit that acquires an evaluation value for a state of cells which are cultured in each of a plurality of fluidic devices, culture environment, and information representing a disposition position of the fluidic device; and a generation unit that generates a learned model in which the evaluation value and the information representing the disposition position are received as an input and the culture environment is output, through machine learning using, as training data, the evaluation value before adjustment of the culture environment, the culture environment after the adjustment, and the information representing the disposition position, in a case where, due to the adjustment, the evaluation value becomes a first threshold value or more and an absolute value of a difference in evaluation value between the plurality of fluidic devices becomes a second threshold value or less.

A system and method for creating mycelium textile materials is disclosed, in which leftover, cutoff, and other materials used to create the textile materials that would otherwise be discarded are further used in a second process to create bonded mycelium boards. The system and method further reuse or recycle materials throughout the process of creating the mycelium textile fabric and bonded mycelium boards, thus keeping waste to a minimum.

The present disclosure provides a HTP microbial genomic engineering platform that is computationally driven and integrates molecular biology, automation, and advanced machine learning protocols. This integrative platform utilizes a suite of HTP molecular tool sets to create HTP genetic design libraries, which are derived from, inter alia, scientific insight and iterative pattern recognition. The HTP genomic engineering platform described herein is microbial strain host agnostic and therefore can be implemented across taxa. Furthermore, the disclosed platform can be implemented to modulate or improve any microbial host parameter of interest.

The present disclosure aims to provide a manufacturing method of a cell structure. The manufacturing method comprises a preparation step of preparing, on a culturing surface of a cell culture container, a first coated region coated with a temperature-responsive polymer and/or a temperature-responsive polymer composition, and a plurality of second coated regions located at an edge of the first coated region and coated with a cell adhesive substance; and a seeding and culturing step of seeding cells in the first coated region and the second coated regions and culturing the cells to produce a cell structure.