A system for performing a molecular analysis workflow includes a reaction holder or a reaction substrate, such as a multi-well reaction plate, with a reaction holder/substrate RFID tag, and/or a reagent container with a reagent container RFID tag, and an instrument and/or device that includes an RFID reader/writer operable to read and/or write information to and from the reaction holder/substrate RFID tag and/or the reagent container RFID tag. The reaction holder/substrate RFID tag and the reagent container RFID tag can be utilized separately or together to send and receive and store information, for example, for a workflow of a molecular analysis, such as a polymerase chain reaction (PCR).

A point-of-care diagnostic system that includes a cartridge and a reader. The cartridge can contain a patient sample, such as a blood sample. The cartridge is inserted into the reader and the patient sample is analyzed. The reader contains various analysis systems, such as an electrophoresis detection system that uses electrophoresis testing to identify and quantify various components of the blood sample. The reader can process data from the various patient sample analysis to provide interpretative results indicative of a disorder, condition, disease and/or infection of the patient.

The present invention relates to a vessel comprising a device, said device being a sensor or an information storage device or both, and a communication means to transfer data from said vessel to a receiver. The present application also relates to a system, for example a storage system, comprising such vessel.

An elution apparatus and a detection apparatus are described. The elution apparatus includes: a sample trap for trapping a sample; and one or more pumps and/or valves to move a liquid eluent and a liquid eluate, wherein the eluate includes an extracted portion of the sample that is extracted by the eluent. The detection apparatus includes: a capillary having a low-voltage (LV) end portion to receive a sample; and a conductivity detector coupled to a high-voltage (HV) end portion of the capillary to generate signals based on conductivity of a monitored portion of the capillary in the HV end portion, wherein the conductivity detector is electrically isolated from the LV end portion.

A system and method for performing a portable, fast, field assay of a small sample biological analyte includes a microfluidic cartridge and a reader with which the microfluidic cartridge is selectively communicated. A closed microfluidic circuit mixes and recirculates the analyte with a buffer. A shear horizontal surface acoustic wave (SAW) detector communicates with the microfluidic circuit and has a plurality of channels including at least one functionalized sensing channel in which the mixed analyte and buffer is recirculated and sensed. Capture of the analyte is amplified by recirculation of the analyte and buffer, and detection is amplified by use of an all-purpose endospore display mass amplification.

Provided is a thermal cycler including a housing, the housing with a thermal block having sample wells, each for receiving a test sample in a sample vessel, an electric heater for heating the thermal block, a power supply and an electronic control for controlling the electric heater, and a temperature analysis and/or verification unit for analyzing and/or verifying a thermal performance of the thermal block. Also provided is a method for analyzing or verifying a thermal performance of a thermal cycler and for calibrating the thermal cycler. The thermal cycler has a temperature analysis and/or verification unit integrated into the housing and connected to the power supply and electronic control by an internal interface, whereas the method is characterized by the following steps: providing the thermal cycler with an integrated temperature analysis and/or verification unit and using the integrated temperature analysis and/or verification unit for self-calibration of the thermal cycler.

Cryogenic devices are provided in which solid carbon dioxide (dry ice) is used to maintain a temperature zone in which samples can be manipulated under conditions in which the sample is maintained at a temperature below 50 C.

The present disclosure relates to retractable diagnostic devices, and hybrid diagnostic devices comprised of water-dispersible, flushable, biodegradable, or water-soluble material and non-water-dispersible, non-flushable, or non-water-soluble material.

Methods and apparatus for providing an isolated single cell are provided. In one disclosed arrangement, a test body of liquid is formed on a substrate surface. A contact angle between the test body of liquid and the substrate surface is lower than an equilibrium contact angle. An optical image of the test body of liquid is analysed to determine whether one and only one cell is present in the test body of liquid.

A lidded vessel made of plastic for treating samples in the laboratory having a vessel having a tubular vessel body, a vessel floor at the bottom, a vessel opening at the top, and a circumferential first sealing region on or near the vessel opening, a lid having a lid floor and a circumferential second sealing region for sealing against the first sealing region, at least one apparatus for releasably attaching the lid to the vessel when the first sealing region is in sealing contact with the second sealing region, wherein the lid has, on the upper side, a series of divisions running around the central axis of the vessel for marking an alignment of the lidded vessel in a laboratory device for treating a sample in the lidded vessel and/or for marking a division representing a sample filled into the lidded vessel and/or for marking a division representing a treatment step of a sample in the lidded vessel.