An automated positive pressure solid phase extraction apparatus and method comprising two tiered lifts devices each individually controllable to individually vertically translate within an elevator framework between a base on which the elevator framework is mounted and a manifold plate supported by the framework in a substantially horizontal plane parallel with and vertically above the two tiered lifts devices; a rectilinearly translating shuttle assembly comprising a shuttle supporting labware for rectilinear travel into and out of the elevator framework to handoff the labware to one of the two tiered elevator lifts or both; and a reagent dispensing system comprising a reagent dispensing manifold for dispensing liquids into wells of each column of wells of a labware filter plate carried by the shuttle.

A sample measurement system according to an embodiment may include: sample measurement units that receive supply of containers and perform measurement on samples; a rack setting unit in which a rack storing the containers to be supplied to at least one of the sample measurement units is set; a first transport path that transports the containers from the rack setting unit to at least one of the sample measurement units; a second transport path that is provided at a position different from the first transport path in a height direction and that transports the containers from at least one of the sample measurement units to the rack setting unit; and a transfer path that transfers the containers between the first transport path and the second transport path.

The present invention provides a production-line-type high-throughput screening system, which relates to the field of biotechnology and testing equipment. The system comprises of four manipulators, three parallel conveyor belts with fixed slots, 2-DOF slipway and fixed fixtures, 96-channel pipetting system, coloring device, oscillating mixing device, microplate reader, well plates loading platform and well plates recycling platform. Manual operation takes five minutes to detect one 96-well plate, while this system can handle 20 96-well plates per minute. It expands the number of screening targets, making the screening process more clearly and concisely and liberating manual labor. The system makes effective contributions to the development of microbial breeding technology.

A high throughput system and method for analyzing the effects of a plurality of agents on planaria is disclosed. Multiple test zones are provided, where each test zone contains at least a portion of one planarian. The planaria in each test zone are then exposed to at least one agent, the test zones are sealed, and at various times, the test zones are moved automatically between a storage location and at least one assay station. At each assay station, the test zones are exposed to a set of conditions, and an image or video of the planaria in the test zones are captured. Automated image or video analysis is used to are evaluate and determine whether the agent has an effect.

A receptacle terminal having a housing, and a first transporting unit which is configured to transport at least a first receptacle rack, which is arranged on a movable platform, within the housing from a first position to a second position, and wherein the first receptacle rack is at the second position within the housing and manually accessible by a user through a first opening in the housing.

An interactive test method, device and system are disclosed. An interactive test method, applicable to a product to be tested, including: obtaining an identification of the product to be tested; obtaining test conditions corresponding to the product to be tested according to the identification, wherein the test conditions include a test type, a test location, a test case and the attribute information of the test case; transmitting a first instruction including the test location to an actuating device; transmitting a second instruction including the test case and the attribute information of the test case to a test device; and obtaining test data transmitted by the test device and obtained by performing a test according to the first instruction and the second instruction, and comparing the test data with the test case to obtain a test result.

A biologic sample preparation system that prepares samples for processing includes a frame defining a horizontal plane, a pipette assembly, a sample module and an extraction module. The pipette assembly includes a first pipette. The pipette assembly is movably mounted to the frame in a direction substantially perpendicular to the horizontal plane during operation. The sample module includes a sample plate and is movably mounted to the frame. The sample module is movable substantially parallel to the horizontal plane at least from a sample area spaced from the pipette assembly and a working area proximate the pipette assembly. The extraction module includes an extraction plate and is movably mounted to the frame. The extraction module is movable substantially parallel to the horizontal plane at least from an extraction staging area spaced from the pipette, assembly and the working area proximate the pipette assembly.

An automated sample inspection system is provided with a conveyance line for conveying sample carriers; an empty sample carrier line for conveying empty sample carriers; and a buffer line for temporarily holding empty sample carriers supplied from the empty sample carrier line to the conveyance line. According to the depletion status of the buffer line of each processing system, and the depletion status of other processing systems adjacent to each processing system, the number of empty sample carriers to be conveyed from the empty sample carrier line to the buffer line of each processing system, and the number of empty sample carriers to be conveyed from the empty sample carrier line of each processing system to the empty sample carrier line of another adjacent processing system are determined. Consequently, delays in the processes in the system can be suppressed due to the suppression of the depletion of sample carriers.

The present invention relates to an analytical device for the elementary analysis, which is improved with regard to the feeding of samples, with a sample holder, a line for oxygen and inert gas, a reactor for catalytic combustion of a sample, a reduction reactor that is provided downstream of the reactor, an adsorber that is provided downstream of the reduction reactor, a detector that is provided downstream of the absorber and a logic unit for processing of the data transmitted by the detector, wherein the sample holder includes a perforated field plate that can be moved by means of a drive on a base that is equipped with an ejection opening to eject one of the samples.

The disclosure provides a to-be-tested object processing apparatus and a nucleic acid testing integrated machine with the to-be-tested object processing apparatus. The to-be-tested object processing apparatus includes: a frame, provided with a sample processing platform; an extraction mechanism, configured to extract an analyte; a grabbing part, movably arranged above the sample processing platform; a transfer part being movably arranged on the sample processing platform, the transfer part including an extraction plate transfer part, the extraction plate transfer part being provided with a first transfer position, the grabbing part being provided with a first grabbing position and a second grabbing position, and when the extraction plate transfer part is located in the first transfer position, the grabbing part being able to move between the first grabbing position and the second grabbing position; and a pipetting part, movably arranged above the sample processing platform, wherein the extraction plate transfer part is further provided with a sample adding position, and when the extraction plate transfer part is located in the sample adding position, the pipetting part is further provided with a first pipetting position.