Patent classifications
B01L3/565
Heat-sealable chemical vapor-sensor bag
The present invention relates to a chemical vapor-sensor bag with an integrated sensor array to verify the presence of specific chemical vapors inside a sealed bag. In an exemplary embodiment, a device can be sealed within a vapor-sensor bag to allow the device to be transported to and tested for contaminants at the point of use by an end user of the device. In another exemplary embodiment, a device can be coupled to a gas port on a vapor-sensor bag to allow gas within the device to be tested for contaminants. In another exemplary embodiment, gas from a device can be streamed through vapor-sensor bag by coupling the device to a first gas port on a vapor-sensor bag and allowing gas to exit the bag through a second gas port.
METHOD FOR PROCESSING POLYNUCLEOTIDE-CONTAINING SAMPLES
Methods and systems for processing polynucleotides (e.g., DNA) are disclosed. A processing region includes one or more surfaces (e.g., particle surfaces) modified with ligands that retain polynucleotides under a first set of conditions (e.g., temperature and pH) and release the polynucleotides under a second set of conditions (e.g., higher temperature and/or more basic pH). The processing region can be used to, for example, concentrate polynucleotides of a sample and/or separate inhibitors of amplification reactions from the polynucleotides. Microfluidic devices with a processing region are disclosed.
INTERLOCKING CAP AND VIAL
A receptacle cap includes a probe recess configured to receive a probe inserted therein to thereby frictionally secure the receptacle cap to the probe, and a closed lower end of the receptacle is insertable into an open end of a reaction receptacle to close the reaction receptacle. The receptacle cap and the reaction receptacle include interlocking features for securing the receptacle cap to the reaction receptacle.
Systems and methods for handling microfluidic droplets
The invention generally relates to assemblies for displacing droplets from a vessel that facilitate the collection and transfer of the droplets while minimizing sample loss. In certain aspects, the assembly includes at least one droplet formation module, in which the module is configured to form droplets surrounded by an immiscible fluid. The assembly also includes at least one chamber including an outlet, in which the chamber is configured to receive droplets and an immiscible fluid, and in which the outlet is configured to receive substantially only droplets. The assembly further includes a channel, configured such that the droplet formation module and the chamber are in fluid communication with each other via the channel. In other aspects, the assembly includes a plurality of hollow members, in which the hollow members are channels and in which the members are configured to interact with a vessel.
CONTAINER AND METHOD FOR ACTIVATING REAGENTS IN SUCH A CONTAINER
The invention discloses a container for reagents for an analyzer in process automation technology, comprising an, in particular bottle-shaped, container wall which is designed to form a first compartment for a first reagent; an insert which is arranged at least in some sections in the first compartment, and which forms a second compartment separated from the first compartment for a second reagent, wherein the insert comprises a closure; and a punch which is movable at least between a first position and a second position, wherein the punch, in moving from the first position to the second position, opens, in particular cuts through, penetrates, pierces or presses out, the closure and clears a path from the second compartment into the first compartment, whereby second reagent enters the first reagent. In addition, the invention also discloses a corresponding method.
Specimen container for biological materials
A specimen container that includes a first cylindrical housing section having a first threaded end, a second threaded end, and a body section formed therebetween, wherein a fill line is placed at a predetermined location on the body section; a threaded winged section that is adapted to be attached to the second threaded end of the first cylindrical housing section, wherein the threaded winged section includes two gripping wings formed on opposite sides of the threaded winged section; a second cylindrical housing section having a first threaded end, a second threaded end, and a body section formed therebetween, wherein two gripping wings are formed on opposite sides of the second cylindrical housing section and are integral therewith; a threaded connector ring that is adapted to connect the first cylindrical housing section to the second cylindrical housing section; and at least one syringe plunger adapted for insertion into the first cylindrical housing section or the second cylindrical housing section.
CONFIGURABLE DEVICE FOR THE FLEXIBLE PROVISION OF COMPOUNDS AND/OR FUNCTIONS IN A BIOPHARMACEUTICAL PROCESS
A configurable device (10) for the flexible provision of connections and/or functions in a biopharmaceutical process comprises a body (20) in which predefined pipe sections (22) and plug-in locations (24) are formed by recesses in the material of the body (20). The configurable device (10) further comprises a plurality of functional elements (26) which are adapted to be inserted into the plug-in locations (24).
Test device and test method
A test device and a test method are provided which can prevent a specimen liquid from splattering and leaking and perform an examination simply and safely. The test device includes a culturing unit configured to be capable of culturing a specimen in a sealed state, a test piece configured to be capable of absorbing a specimen liquid in the culturing unit, a separating unit configured to be capable of separating the test piece and the specimen liquid in a non-contact state, an opening unit configured to be capable of opening at least a portion of the separating unit to form a flow path through which the specimen liquid reaches the test piece, and a case configured to integrally seal at least a portion of the test piece on a side closer to the separating unit, at least a portion of the culturing unit, and the separating unit.
INTERLOCKING CAP AND VIAL
A cap that is securable to a vial includes a plug configured for insertion into an open end of the vial. An upper portion of the cap defines a probe recess with an open top end and configured to receive a distal end of a probe of a pipettor inserted into the open top end, to frictionally secure the cap to an end of the probe. The cap includes a radially-oriented annular surface with one or more locking members depending from a periphery of the annular surface. The locking members are spaced from the plug and each locking member includes a radial locking groove and a radial locking ridge beneath the radial locking groove. A lip of the vial snaps into the radial locking groove above the radial locking ridge to secure the cap to the vial when the plug is inserted into the open end of the vial.
SYSTEM AND METHOD FOR CONDUCTING AN ASSAY
A system for performing a nucleic acid amplification assay comprises a thermally-conductive receptacle holder with one or more receptacle wells, each conforming to an outer surface of a lower portion of a vial. A through-hole extends from an inner surface of each well to an outer surface of the holder. A thermal element is positioned proximal to the holder for altering a temperature of the holder. A signal detection module is configured to generate an excitation signal directed through the through-hole of the well and detect an optical emission from a fluid contained in the vial supported by the well. At least one well supports a capped vial containing a reagent for a nucleic acid amplification assay and including an opaque cap sealing an open end of the vial. The lower portion of the vial is contained within a well, and the cap is situated above a top surface of the holder.