Embodiments in accordance with the present disclosure are directed to apparatuses used for reaction screening and optimization purposes. An example apparatus includes a plurality of reaction vessels, a dispensing subsystem, at least one reactor module, an analysis subsystem, an automation subsystem, and control circuitry. The dispensing subsystem delivers reagents to the plurality of reaction vessels for a plurality of reaction mixtures having varied reaction conditions. The at least one reactor module drives a plurality of reactions within the plurality of reaction vessels. The analysis subsystem analyzes compositions contained in the plurality of reaction vessels. The automation subsystem selectively moves the plurality of reaction vessels from a location proximal to the dispensing subsystem to the at least one reactor module based on experimental design parameters. And, the control circuitry identifies optimum reaction conditions for a target end product based on the analysis.

Methods and systems for solid phase extraction procedures are provided. Methods and systems of the present disclosure provide for improved accuracy, automation, and ease of use of various solid phase extraction procedures and other processes to be performed in a laboratory setting. Systems and methods for fluid flow regulation and detection are disclosed.

Closing arrangement for a cap of a tube in a carrier, wherein the arrangement comprises at least a first, a second and a third moveable engagement member, the first member being adapted to induce a first part of the cap rotation and the second member being adapted to induce a second part of the cap rotation and the third member being adapted to induce a third part of the cap rotation for closure.

A storage system for storing material such as sample tube caps comprises a drawer with a reservoir, the drawer being movable between a first position and a second position. A storage container is arranged below the reservoir of the drawer when the drawer is arranged in the first position. A transport device is configured to retrieve material from the storage container and to transport the material out of the storage container. Therein, the reservoir of the drawer comprises a bottom with at least one closable opening.

According to an embodiment, a cap-closing apparatus includes, a holding mechanism section configured to be capable of holding a cap which is attached to an opening of a specimen container that is formed to be capable of containing a specimen, a moving mechanism section configured to move the cap, a rotating mechanism section configured to rotate the cap, a torque detector configured to detect a torque at a time of rotation, and a controller configured to control an amount of rotation of the rotating mechanism section, based on the torque detected by the torque detector.

A reagent bottle includes an outer cap and an inner closing cap. The inner closing cap has a recess for gripping the cap. In addition, a system for handling closures is provided wherein a method removes a closing cap from a reagent bottle and a related gripper.

Systems and methods for detecting and/or identifying target cells (e.g., bacteria) using engineered transduction particles are described herein. In some embodiments, a method includes mixing a quantity of transduction particles within a sample. The transduction particles are associated with a target cell. The transduction particles are non-replicative, and are engineered to include a nucleic acid molecule formulated to cause the target cell to produce a series of reporter molecules. The sample and the transduction particles are maintained to express the series of the reporter molecules when target cell is present in the sample. A signal associated with a quantity of the reporter molecules is received. In some embodiments, a magnitude of the signal is independent from a quantity of the transduction particle above a predetermined quantity.

Automated apparatus and methods for dispensing fluids into microplates utilizing microwell covers, the covers comprising open portions to allow a pipette access to one or more wells and impermeable portions which prevent the fluids from getting into wells shielded by the impermeable portion. The open portions and impermeable portions are preferably arranged and sized to align with alternating rows of wells in a particular microplate. Preferred covers are movably positioned on the microplate. Automated dispensing apparatus for use with microplates and microwell covers comprises a programmable controller, and suitable interfaces which allow the apparatus to be programmed, and which control a dispensing head such that pipettes are moved in the desired manner in order to take advantage of the protective features of the microwell covers. The apparatus also preferably comprises at least one transfer mechanism for moving a cover relative to a microplate at a dispensing station.

A vacuum assist apparatus can comprise a microplate. The microplate can comprise a first surface and an opposing second surface. A plurality of wells can be formed in the first surface of the microplate. Each of the plurality of wells can be sized to receive an assay therein. A support base can comprise a fluid passage. The microplate can be positioned adjacent and in contact with the support base. A pressure device, in fluid communication with the fluid passage, can exert a vacuum within the fluid passage to actively retain the microplate in the contact with the support base.

A method for capping vessels containing biological samples is described providing a cap supply with a plurality of caps for the vessels within compartments in a predefined geometrical arrangement. The cap supply is introduced through an interface into a preanalytical system including a housing, and is reversibly docked to a feeder for inserting the cap supply into the preanalytical system and retrieving it therefrom. Subsequently, a cap is retrieved from the supply by a robotic manipulator, and transported to a workstation holding the vessels. A vessel is then capped using the manipulator. The steps from introducing the cap supply into the preanalytical system to capping a vessel are repeated a certain number of times or until all caps of the supply have been retrieved. Finally, the cap supply is retrieved from the preanalytical system. A preanalytical system and a cap supply for capping vessels containing biological samples is also provided.