The processing apparatus 200 of the present disclosure includes: a laser irradiation unit 21 capable of applying a laser to the photothermal conversion layer 13 of the cell culture tool 100 including the cell culture base layer 11 and the photothermal conversion layer 13; and a control unit 22 for controlling the laser irradiation unit 21. The control unit 22 includes a setting section 221 and an irradiation control section 222. The setting section 221 sets an irradiation region to be irradiated with the laser in the cell culture tool 100. The irradiation control section 222 controls the laser irradiation unit 21 based on the irradiation region such that the laser irradiation unit 21 applies the laser to a corresponding region of the photothermal conversion layer 13.

A cell culture method is a cell culture method for arranging cultured cells in a culture dish and continuously culturing the cultured cells by supplying a liquid required to grow or maintain the cultured cells to the culture dish and discharging the liquid from the culture dish. The cell culture method includes: providing a supply port of the liquid at one end of the culture dish and providing a discharge port of the liquid at other end of the culture dish so as to sandwich the cultured cells between the supply port and the discharge port, and discharging the liquid while supplying the liquid to the culture dish so that a moving linear velocity of the liquid from the supply port toward the discharge port is less than a maximum velocity at which shear stress is not applied to the cultured cells.

An imaging system and method for microbial growth detection, counting or identification. One colony may be contrasted in an image that is not optimal for another type of colony. The system and method provides contrast from all available material through space (spatial differences), time (differences appearing over time for a given capture condition) and color space transformation using image input information over time to assess whether microbial growth has occurred for a given sample.

The present invention relates to systems and methods involving interconnected plate components, including bases, lids and covers, interconnected in a manner such that a continuous strip of each component is prepared. The continuous strips may be stored as rollstock in a reel style. The physical properties of each continuous strip allow the base, lid and/or cover to include means for positive control. In one embodiment, the continuous strip of bases is advanced and processed through an automated system with positive control, and remains in the form of a continuous strip until agar in the bases is cured, at which time the bases are singulated. When a lid is applied to a base using methods described herein, an airtight seal is formed improving the quality of culture media used in testing.

A Petri dish (100) base (300) and lid (200) each having a substantially circular, substantially flat region from which sidewalls extend perpendicular to the flat region (312) forming a corner (326), (230). The base may have a base stacking ring (325) extending from the base (300) at the corner (326), and an internal channel (330) around the inside of the base (300) at the corner (326). The base (300) may have a uniform cross-sectional thickness (350) and may also have vents (322) in the base stacking ring (325). The lid (200) may have a uniform cross-sectional thickness (250). The lid (200) may have a lid stacking ring (225) at the corner (230), which forms a groove (240) in the interior (212) of the lid (200) at the corner (230). The lid may also have ribs (295) and vents (222) to enable multiple dishes to be stacked without forming a vacuum.

The present invention provides a culture vessel and a measuring device for measuring a cell sheet thickness nondestructively during culturing. A culture vessel having a lid 4 has a float 8 installed in the interior and the float is structured so as to be uplifted by a culture medium in the culture vessel. Further, a cell sheet thickness measuring device having a sensor head 10 having a light-emitting element 10A and a light-receiving element 10B to detect a positional variation of the float in the vertical direction and a controller 11 to process a signal of the sensor head is configured.

An imaging system and method for microbial growth detection, counting or identification. One colony may be contrasted in an image that is not optimal for another type of colony. The system and method provides contrast from all available material through space (spatial differences), time (differences appearing over time for a given capture condition) and color space transformation using image input information over time to assess whether microbial growth has occurred for a given sample.

An apparatus for conveying a plurality of articles includes a transport belt, a bumper stopper, and a rotator. A motor moves the transport belt which is adapted to rotate the rotator as the belt conveys the plurality of articles. The stopper can move between first and second positions relative to the transport belt wherein the bumper stopper guides one article toward the rotator when the bumper stopper is in the first position. The bumper stopper allows the article to be conveyed to another location when the bumper stopper is in the second position. The transport belt can continue to convey other articles while the one article is temporarily held in place by the bumper stopper. The rotator is configured to rotate the article conveyed by the transport belt. The article can remain in contact with the transport belt while the rotator is rotating the article.

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.

Treatment of wastewater and particularly relates to a technique for wastewater treatment using renewable energy (RE) which is sole solar energy (SE). In bench scale experiment, a device is constructed to consist of two fixed upper and lower glass Petri dishes. Another device consists of plastic containers and both devices with the same volume of wastewater in the upper and distilled water in the lower container. The first device is placed on the bench beside window to be exposed to sunlight at room temperature and the other device is put outdoors under direct sunlight during daytime. A build-up of small circular water droplets starts to appear on the external bottom of upper container. Water droplets are allowed to fall freely in the lower container, pH of droplets water is about 7.1. Yield of freshwater is at a rate of approximately 300 ml freshwater from 400 ml wastewater per 48 hours.