A sample carrier device including a single substrate, a penetration structure and a fixing structure is provided. The penetration structure is formed on a side of the substrate. The penetration structure has a fluid passage. The fixing structure is formed on a side of the penetration structure. The sample carrier device is divided into an end portion, an observation portion and an operation portion. The user can separate the observation portion from the end portion by operating the operation portion. After the observation portion is separated from the end portion, the user can inject the sample into the fluid passage through a port of the fluid passage exposed to the observation portion. Once the sample is carried by the fluid passage of the observation portion, the user can seal the port of the fluid passage and place the observation portion in an electron microscope device.

Disclosed is a specimen treatment device for treating a specimen accommodated in a reaction container, the specimen treatment device comprising: an installation unit in which the reaction container is installed; a temperature adjusting unit for warming the reaction container installed in the installation unit; and an opening/closing member which can move between a first position at which the temperature adjusting unit is uncovered and a second position at which the temperature adjusting unit is covered.

The present technology provides for a fluorescent detector that is configured to detect light emitted for a probe characteristic of a polynucleotide. The polynucleotide is undergoing amplification in a microfluidic channel with which the detector is in optical communication. The detector is configured to detect minute quantities of polynucleotide, such as would be contained in a microfluidic volume. The detector can also be multiplexed to permit multiple concurrent measurements on multiple polynucleotides concurrently.

The present technology provides for an apparatus for detecting polynucleotides in samples, particularly from biological samples. The technology more particularly relates to microfluidic systems that carry out PCR on nucleotides of interest within microfluidic channels, and detect those nucleotides. The apparatus includes a microfluidic cartridge that is configured to accept a plurality of samples, and which can carry out PCR on each sample individually, or a group of, or all of the plurality of samples simultaneously.

A thermal cycler system for use with a sample holder configured to receive a plurality of samples includes a sample block configured to receive the sample holder, a cover lid configured to move in a direction toward the sample block from an open position to a closed position, a heated cover operatively coupled to the cover lid and configured to move in a direction toward the sample block from a raised position to a first lowered position, in which the heated cover contacts the sample holder when the sample holder is received by the sample block, and a drive assembly including a motion guide configured to move in a direction toward the sample block from a first position, wherein the cover lid is in the open position and the heated cover is in the raised position, to a second position, wherein the cover lid is in the closed position.

A heater (22) for heating a substantially transparent or translucent cover of a reaction vessel. The heater has a board (80) having a front face, an opposing back face, and an aperture (1062) through which an excitation beam can pass into a reaction vessel via a cover of the reaction vessel, and/or through which reaction light can pass from the reaction vessel via the cover. A thermally conductive, heat-spreading layer (86) radiates heat towards the cover, the heat-spreading layer being arranged on the front face of the board that is arranged to face the cover. At least one heating element outputs heat to the heat-spreading layer (86), the heating element being arranged on the back face of the board that is arranged to face away from the cover. The heat-spreading layer (86) is in thermal communication with the heating element by at least one heating via 82 through the board.

Provided herein are devices, methods, and systems for polynucleotide synthesis comprising a thermocycler comprising a plurality of individual chambers having a capability to control its own temperature setting and a machine learning for generating a recommendation of a design of experiment for polynucleotide synthesis.

A reagent storage device of the present disclosure includes a shutter and a moving mechanism. The shutter is configured to open and close an opening in a reagent compartment for housing a reagent container, the reagent compartment being provided with the opening for insertion and removal of a probe used to extract a reagent from inside the reagent container housed in the reagent compartment. The moving mechanism is configured to move the shutter to an overlay position opposing the opening and separated from the opening before moving the shutter downward so as to close off the opening, and is also configured to move the shutter that is closing off the opening upward to open up the opening before withdrawing the shutter from the overlay position over the opening.

An apparatus for holding sample tubes for sample preparation is provided. The apparatus includes a sample tube holder with an opening to accept a sample tube. The apparatus includes a hinge assembly with a hinge plate and a hinge support, wherein the hinge plate is movable relative to the hinge support. In one example, the hinge plate pivots in two rotation directions and slides in two translational directions relative to the hinge support. The hinge plate limits vertical movement of the sample tube within the sample tube holder. In one aspect, a method includes inserting a sample tube into an opening of a sample tube holder and pivoting and sliding a hinge plate relative to a hinge support, wherein the hinge plate limits vertical movement of the sample tube within the sample tube holder.

A device and a method for isolating a target from a biological sample are provided. The target is bound to solid phase substrate to form target bound solid phase substrate. The device includes a lower plate with an upper surface having a plurality of regions. The biological sample is receivable on a first of the regions. An upper plate has a lower surface directed to the upper surface of the lower plate. A force is positioned adjacent the upper plate and attracts the target bound solid phase substrate toward the lower surface of the upper plate. At least one of the upper plate and the lower plate is movable from a first position wherein the target bound solid phase substrate in the biological sample are drawn to the lower surface of the upper plate and a second position wherein the target bound solid phase substrate are isolated from the biological sample.