A method of processing and storing biological cells includes introducing a flowable medium into a microfluidic device, the flowable medium including biological cells; sequestering one or more biological cells from the flowable medium in one or more isolation regions of the microfluidic device; and freezing the microfluidic device including the one or more biological cells sequestered therein.

The invention relates to a method for controlling a thermal cycler and a thermal cycler, in which the determination of at least one temperature change rate is carried out by an evaluation program using tempering schedule data and run time data, whereby in particular the tempering behavior of a slower thermal cycler can be simulated on a faster thermal cycler.

Tamper-resistant and tamper-evident sample bottles for the transport of pressurized well fluid include sensor packages and data recording devices to characterize and track properties of the sample bottle and its contents.

A diagnostic and treatment assembly, configured to diagnose and treat cellular disease. The diagnostic and treatment assembly has a radio wave generator communicatively coupled to a carrier modulator and a radio wave amplifier. An impedance matching system is electrically coupled to the radio wave amplifier. A reflected wave sensor is electrically coupled to the impedance matching system. A radiator applicator is electrically coupled to the reflected wave sensor. A vector impedance analyzer is electrically coupled to the radio wave amplifier. An information collector data network is electrically coupled to the vector impedance analyzer. A data logger is communicatively coupled to the carrier modulator, the vector impedance analyzer, and the reflected wave sensor. The diagnostic and treatment assembly operates in a low-power mode to diagnose a cellular disease and in a high-power mode to treat the cellular disease.

A sensor device for detecting transport parameters representative of those experienced by a sample during transportation is provided. The sample is stored in a container. The sensor device includes a housing with a configuration that generally matches the configuration of the container, a hardened substrate portion formed from a substrate material, and a sensor assembly comprising at least one sensor for detecting at least one transport parameter (e.g. acceleration, orientation, temperature, etc.). The sensor assembly is secured within the housing by the hardened substrate portion. Optionally, a weight of the device approximates a combined weight of the container and the sample stored therein. The weight of the sensor device can be adjusted. When the device is positioned proximate to the container during transportation, the at least one transport parameter detected by the at least one sensor is analogous to that at least one transport parameter experienced in the container.

A device and a method for the extraction of nucleic acids from samples comprising cells. The invention provides a consumable for handling liquids in automated analyser systems, comprising a plurality of cavities which are connected by a bridge, wherein the bridge defines a horizontal axis which connects the plurality of cavities, which are arranged in a straight line and wherein at least one cavity of the plurality of cavities is shaped to accommodate a pipette tip, and a handling interface, which is attached to the bridge. A device comprising the consumable and a method for using the consumable.

A holding portion includes a first holding portion and a second holding portion that respectively hold a first cassette holder and a second cassette holder, a chemical liquid bottle holding portion including a first chemical liquid bottle holding portion and a second chemical liquid bottle holding portion, and a paraffin-filled bottle holding portion including a first paraffin-filled bottle holding portion and a second paraffin-filled bottle holding portion. The first cassette holder is inserted into the chemical liquid bottle provided to the first chemical liquid bottle holding portion and the paraffin-filled bottle provided to the first paraffin-filled bottle holding portion. Furthermore, the second cassette holder is inserted into the chemical liquid bottle provided to the second chemical liquid bottle holding portion and the paraffin-filled bottle provided to the second paraffin-filled bottle holding portion.

Assay cartridges are described that have a detection chamber, preferably having integrated electrodes, and other fluidic components which may include sample chambers, waste chambers, conduits, vents, bubble traps, reagent chambers, dry reagent pill zones and the like. In certain embodiments, these cartridges are adapted to receive and analyze a sample collected on an applicator stick. Also described are kits including such cartridges and a cartridge reader configured to analyze an assay conducted using an assay cartridge.

A processing system includes a processing unit configured to process a cartridge, in particular a microfluidic cartridge, and is further configured to process a biological sample received in the cartridge. The processing unit includes a computing unit configured to compare input or read in sample data with input or read in first cartridge data in order to determine a compatibility of the sample with the cartridge. The computing unit is further configured to output a first error message in response to a determination of incompatibility between the sample and the cartridge. A method includes using the processing system to determine a compatibility between a sample and a cartridge.

Systems and methods are described for quantifying a target nucleic acid. A sample comprising a target nucleic acid is segregated into a first plurality of the reaction volumes containing at least one target nucleic acid molecule and a second plurality of the reaction volumes containing no target nucleic acid molecules. The reaction volumes are subjected to an amplification assay, wherein the amplification assay is configured to amplify the target nucleic acid. An indicator of amplification is detected or measured in at least some of the plurality of reaction volumes. The target nucleic acid is quantified based on the detection or measurement. After discontinuing the amplification assay, the plurality of reaction volumes may be heated and changes in the indicators of amplification of two or more of the at least some of the reaction volumes may be detected or measured.