An automatic analysis device has a plurality of types of photometers having different quantitative ranges, and an analysis control unit for quantifying the desired component in specimens based on measurement values of one or more photometers selected from among the plurality of types of photometers. The analysis control unit: sets a switching region in an overlap region of respective quantitative ranges of the plurality of types of photometers, said switching region having a greater width than does the variation in quantitative values of the desired component based on the measurement values of photometers having the same specimen; compares the quantitative value of a quantitative range portion that corresponds to the switching region and the quantitative values of the desired component based on the measurement values of the photometers; and selects a photometer to be used in quantitative output of the desired component from among the plurality of types of photometers.

The present invention relates to novel modules for transferring magnetic beads, an automated system comprising the same and a method for extracting nucleic acids using the same. The specifically designed magnet module and cover module of the present invention can be employed in the automated liquid handling apparatus by means of pre-existing moving modules (e.g., pipettor module) of the apparatus. The present invention enables a bead transfer-type method for extracting nucleic acids to be performed in an automated manner on the automated liquid handling apparatus. The present invention provides advantages of higher level of automation, more reduced cost and no need for another separate liquid handling apparatus compared to the conventional bead transfer-type method usually performed in the small apparatus designed to be used only for this bead transfer-type method. Also, the present method has the merits of more shortened reaction time compared to the conventional liquid transfer-type method.

The present invention provides methods and devices for simple, low power, automated processing of biological samples through multiple sample preparation and assay steps. The methods and devices described facilitate the point-of-care implementation of complex diagnostic assays in equipment-free, non-laboratory settings.

A quality control sample measurement method, a sample analysis device and a supply device capable of normally acquiring a measurement result of a quality control sample are provided. The quality control sample measurement method for measuring a quality control sample stored in a cold state includes a step of stirring the quality control sample in a first operation mode (step S2) and a step of measuring the stirred quality control samples (step S3). The stirring in the first operation mode differs from the stirring in the second operation mode for stirring the subject sample collected from the subject.

An automated analyzer includes a rod-like member 12a, a driving portion 12c, and a control mechanism 30. The driving portion 12c lifts and lowers the rod-like member 12a a direction of being inserted into and removed from the container 24. The control mechanism 30 controls the driving portion 12c so that the rod-like member 12a is lifted after being lowered so that a tip portion of the rod-like member 12a reaches a first position in the liquid L, and at a time when the rod-like member 12a reaches a second position where the tip portion is not separated from the liquid, an upward motion of the rod-like member 12a is stopped for a given period of time to reduce liquid film adhering to the rod-like member.

The present invention provides an auto biochemical analyzer and a sampling device and a sampling method thereof. The auto biochemical analyzer comprises a frame (100), a horizontal motion system, a vertical motion system, a sampling component and a transfer guide track (101), wherein the horizontal motion system comprises a first stepping motor (116); the vertical motion system comprises a second stepping motor (103); the first stepping motor (116) and the second stepping motor (103) are fixedly installed on the frame (100) respectively; the sampling component comprises a sampling needle holder block (114) and a sampling needle (111); and the stepping motors (116, 103) are both fixed to the frame. The analyzer is smart in motion, low in cost and compact in structure, and has the functions of open sampling and closed puncturing as well as conveying a sample to a specific position.

A microscope slide holder comprising a slide support member and at least one acoustic source for introducing acoustic waves to a microscope slide in communication with the slide support member such that one or more fluids present on the surface of the microscope slide are contactlessly mixed.

An automatic biochemical analyzer, comprises a reaction wheel comprising an inner ring and an outer ring, wherein the reaction wheel is equally divided into multiple cuvette positions along a circumferential direction; the inner ring and the outer ring, respectively, each have a photoelectric detection position, a sample injecting position, a reagent injecting position, a sample stirring position, a reagent stirring position, and a cuvette cleaning position; the photoelectric detection position of the inner ring and the photoelectric detection position of the outer ring have a cuvette position interval of N along a counterclockwise or clockwise direction; and the sample injecting positions, the reagent injecting positions, the sample stirring positions, and the reagent stirring positions of the inner ring and the outer ring, respectively, have a cuvette position interval of M along the same direction, M and N being natural numbers, and the difference between M and N being 0 or 1.

An embodiment of a device for automatically executing a process of generating an emulsion containing nucleic acids, amplifying the nucleic acids in the emulsion, breaking the emulsion, and separating and purifying said amplified nucleic acids, is described that comprises an emulsion generation unit for sealing beads to which nucleic acids are bound in a water-in-oil type emulsion; a nucleic acid amplification unit provided with a reaction vessel for amplifying said nucleic acids and a heating and cooling part for heating and cooling the reaction vessel; an emulsion breaking unit for breaking the emulsion after nucleic acid amplification; and a nucleic acid purification unit for recovering said amplified nucleic acids from said emulsion breaking unit.

Provided herein are methods and systems of the invention that include the use of an automated solution dispenser to form a solution according to at least one target characteristic. A controller may be operatively connected to the automated solution dispenser, wherein the controller is programmed to direct mixing of one or more solids and one or more liquids to produce the solution. At least a portion of the solution can be dispensed into one or more containers.