Methods and devices for single cell analysis using fluorescence lifetime imaging microscopy (FLIM) are disclosed. The methods utilize microfluidic devices which use traps to immobilize cells for FLIM analysis. The analysed cells may be sorted before or after imaging and may be plant, animal, or bacterial cells. Analysis of the FLIM data may use a phasor plot and may be used to identify a metabolic pattern of the single cells.

Device and method for extraction of nucleic acids, comprising a hollow body, preferably a pipette tip, through which a liquid is passed, characterized in that a material with rough or structured surface is disposed in this hollow body in such a way that it can be circumcirculated by a liquid. After lysis of the sample and adjustment of necessary binding conditions for adsorption of the nucleic acids on the carrier material, the mixture, by means of pipetting processes, is repeatedly pipetted along the material for binding nucleic acids, introduced vertically in the pipette tip. The nucleic acids bind to the material. Thereupon washing buffers are likewise pipetted along the material for binding nucleic acids. Then a drying step is performed. Finally, the eluent is again repeatedly pipetted along the vertically disposed material for binding nucleic acids, and in the process the bound nucleic acid is detached. The nucleic acid is now available for necessary downstream application.

The present invention is directed to providing a cryogenic storage device and system that can be regulated at a constant temperature for cryopreservation of biological materials. A cryogenic storage system for cryopreservation of biological materials is provided that may include a storage beaker having at least one storage chamber formed therein, a cooling source, and a cold finger that may be configured to thermally couple the storage beaker to the cooling source.

The present invention is directed to providing a cryogenic storage device and system that can be regulated at a constant temperature for cryopreservation of biological materials. A cryogenic storage system for cryopreservation of biological materials is provided that may include a storage beaker having at least one storage chamber formed therein, a cooling source, and a cold finger that may be configured to thermally couple the storage beaker to the cooling source.

A point of use analyzer includes pump, valve, port, and storage channel. The storage channel may hold multiple assay packets composed of reagent aliquots separated by bounding slugs. The storage channel may define an elongated lumen having two ends with each of the ends coupled to the valve. A sampling device for use with the analyzer engages the port and may include a recurrent coaxial tube having a separation medium. A method of using the analyzer with the sampling device includes steps of pumping a fluid to displace a sample into the separation medium and out through the opposed connection.

Suggested is a method for the extraction of fragrances from natural starting material consisting of the following steps: (a) providing a sample of the natural starting material in a pressure proof sample container; (b) bringing in the sample in contact with liquefied petroleum gas of propane and/or butane gas, preferably; (c) extracting the fragrances from the natural starting material provided in step (b); (d) venting of the pressure proof sample container, while the liquefied petroleum gas is evaporated and the fragrances is maintained as residue in the container; and optionally (e) dissolving the fragrances in a suitable solvent.

An anti-evaporation tube for use with an in vitro diagnostics automation system is provided. The anti-evaporation tube includes an anti-evaporation tube body configured to be automatically inserted in a container and to limit evaporation of one or more fluids in the container and an alignment portion disposed on the anti-evaporation tube body. The alignment portion is configured to automatically align the anti-evaporation tube body within the container and cause the anti-evaporation tube body to remain aligned within the container. The alignment portion includes one or more openings disposed on an upper area of the anti-evaporation tube body. The one or more openings are configured to provide ventilation.

The present invention relates to a soft stopper penetrating dispensing device and a soft stopper penetrating dispensing method. A purpose of the present invention is to suction and discharge liquid with respect to a soft stopper sealed container sealed with a soft stopper such as a rubber stopper without removing the soft stopper. The soft stopper penetrating dispensing device includes a dispensation available punching head which is provided to be relatively movable relative to a stage where the soft stopper sealed container sealed with the soft stopper is able to be placed, a punching tip which has a through-hole along the vertical direction and is made of a hard material and formed in a tapered shape, a dispensing needle tip which is movably provided relative to the head by the dispensing moving mechanism provided in the dispensation available punching head and is able to suction and discharge the liquid.

An observation container (10) includes: a bottom portion that includes a bottom wall (12A) (first plate part) and a bottom wall (12B) (second plate part) which intersect each other and that is configured to accommodate a liquid sample O as a sample containing microparticles to be imaged by imaging units (30A) and (30B) serving as an imaging device; and a region that has transparency with respect to a wavelength of light used for observation of the microparticles.

The invention relates to a collection assembly (1) for small amounts of body fluids, comprising a sample container (2) and an extender element (3). The sample container (2) has a base (13) and a container wall (5) with a first container wall section (6) and a second container wall section (7) adjoining same. The second container wall section (7) is formed hollow-conically and projects into the extender element (3). Moreover, a coupling device (25) with a first coupling element (26) and a second coupling element (27) is provided. When the coupling elements (26, 27) are in coupled engagement, the extender element (3) is coupled to the sample container (2) in a positively locked manner in the form of a snap connection establishing the collection assembly (1).