A system and method for processing and detecting nucleic acids from a set of biological samples, comprising: a capture plate and a capture plate module configured to facilitate binding of nucleic acids within the set of biological samples to magnetic beads; a molecular diagnostic module configured to receive nucleic acids bound to magnetic beads, isolate nucleic acids, and analyze nucleic acids, comprising a cartridge receiving module, a heating/cooling subsystem and a magnet configured to facilitate isolation of nucleic acids, a valve actuation subsystem configured to control fluid flow through a microfluidic cartridge for processing nucleic acids, and an optical subsystem for analysis of nucleic acids; a fluid handling system configured to deliver samples and reagents to components of the system to facilitate molecular diagnostic protocols; and an assay strip configured to combine nucleic acid samples with molecular diagnostic reagents for analysis of nucleic acids.

Provided is a gene amplification apparatus. The gene amplification apparatus includes a supply roller, a roll-type film chip which has a plurality of polymerase chain reaction (PCR) chambers, with which PCR samples are filled, and is wound around the supply roller, a heating roller configured to rotate after being pressed against the film chip and then induce a PCR, a plurality of heating blocks which are disposed on a circumferential surface of the heating roller at preset intervals and brought into contact with the film chip, and a discarding roller configured to discard the film chip which passes the heating roller and on which the PCR is performed.

Analytic sensors and methods utilize an attenuated total reflection (ATR) crystal to detect volatile compounds in an arrangement that reduces interference from compounds other than the one of interest. In particular, the components in the measurement stream are limited to those having volatilities close to that of the analyte of interest, which may be identified based on, for example, the temperature of the ATR crystal and the “dwell time”—i.e., an interval of substantially constant temperature as the ATR crystal is heated.

Magnetic levitation particle separation systems and methods for use with multi-channel flow cells. The system may include a core for receiving and holding the flow cell, with upper and lower clamps for securing the flow cell and positioning it relative to an array of magnets. The system is configured to image particle separation in processing channels of the flow cell, and to regulate the flow cell's temperature. The core may be removable as a single unit, facilitating reconfiguration of the system.

Systems, methods, and collection devices are disclosed for rapid, local PCR testing. The PCR testing system may be configured for use with a disposable sample collection device that includes a swab configured for collecting a biological sample from a patient; and a sample container configured to receive the swab and separate a bulk quantity of the biological sample from the swab for containment in a bulk collection chamber, which is located with the sample container, wherein the sample container is configured to meter a selected volume of the biological sample into a PCR sample tube, which contains a lyophilized master mix, releasably attachable to the sample container.

This invention relates generally to devices, systems, and methods for performing biological assays by using indicators that modify one or more optical properties of the assayed biological samples. The subject methods include generating a reaction product by carrying out a biochemical reaction on the biological sample introduced into a device and reacting the reaction product with an indicator capable of generating a detectable change in an optical property of the biological sample to indicate the presence, absence, or amount of analyte suspected to be present in the sample.

Provided herein are systems and methods for a point of care apparatus. The point of care apparatus includes a fluid container for receiving a biosample, an intermediate cap, and a cartridge having at least one microfluidic channel.

A biological material manufacturing device according to an embodiment of the inventive concept includes a main body and a head unit that is rotatable on the main body. The main body includes a main groove and a first container groove connected to the main groove. The head unit includes a pillar provided in the main groove and a protruding part that protrudes from the pillar.

The present disclosure relates to a portable RT-PCR device and an RT-PCR measurement method that uses the portable RT-PCR device. The portable RT-PCR device includes: a base unit in which a mounting space is formed; a plurality of lower heating units mounted in the mounting space in the base unit; a lower optical measurement unit mounted in the base unit and arranged in a different position than the plurality of lower heating units and providing measurement light or receiving the measurement light; and a chamber assembly including a plurality of chambers that are seated on the plurality of lower heating units and the lower optical measurement unit, respectively, each chamber being provided in such a manner to be movable from one of the plurality of lower heating units to other one of the plurality of lower heating units or to the lower optical measurement unit, wherein each of the plurality of chambers includes: a chamber body for accommodating a chamber unit in which a specimen-unit accommodation space inside which a specimen unit is accommodated is formed; wherein the chamber unit includes: a chamber unit body in which the specimen-unit accommodation space is formed; and a cap unit covering the specimen-unit accommodation space in the chamber unit body from above, and wherein the specimen unit has an aspect ratio, that is, a height-to-width ratio, which is greater than 0 and smaller than 1.

A reaction processing vessel includes a substrate and a groove-like channel formed on the upper surface of the substrate. The channel includes a high temperature serpiginous channel, a medium temperature serpiginous channel, and a high temperature braking channel and a medium temperature braking channel that are adjacent to the high temperature serpiginous channel and the medium temperature serpiginous channel, respectively. The respective cross-sectional areas of the high temperature braking channel and the medium temperature braking channel are larger than the respective cross-sectional areas of the high temperature serpiginous channel and the medium temperature serpiginous channel, respectively.