A sample extraction cassette and method are provided to test for a target in a sample. The sample is obtained on a swab. The swab is inserted into a chamber in a case and into contact with a contact portion of a membrane. The contact portion of the membrane is axially moved into sequential communication with a wash fluid and a reaction fluid. The reaction fluid reacts with the target to provide a visual display corresponding to the presence of the target.

A sample container cap (or “cap”) is configured to be used with a sample container for collecting fluids. The cap has a body and a shutter connected to the body. The cap has a (1) first, open position in which at least one body opening and at least one shutter opening are not aligned and the cap is configured so that fluid cannot readily pass therethrough, (2) second, open position in which the at least one body opening and the at least one shutter opening are aligned and the cap is configured so that fluid can pass therethrough, and (3) third, closed and locked position, in which the at least one shutter opening and the at least one body opening are not aligned and fluid cannot readily pass through the cap, and the cap is configured to not be moved to an open position.

An example method includes reacting a first solution and a different, second solution on a flow cell by flowing the first solution over amplification sites on the flow cell and subsequently flowing the second solution over the amplification sites. The first solution includes target nucleic acids and a first reagent mixture that comprises nucleoside triphosphates and replication enzymes. The target nucleic acids in the first solution transport to and bind to the amplification sites at a transport rate. The first reagent mixture amplifies the target nucleic acids that are bound to the amplification sites to produce clonal populations of amplicons originating from corresponding target nucleic acids. The amplicons are produced at an amplification rate that exceeds the transport rate. The second solution includes a second reagent mixture and lacks the target nucleic acids. The second solution is to increase a number of the amplicons at the amplification sites.

Devices, systems, and methods for storing and/or transporting bodily fluid samples are disclosed herein. In some embodiments, a device for storing and/or transporting a sample of bodily fluid is configured to receive a collection cartridge including a housing and a sample tray removably coupled to the housing. The device can include a base and a cover pivotally coupled to the base. The cover is movable relative to the base between.an open position in which the jig portion is accessible and a closed position in which the jig portion is inaccessible. The base can include a jig portion configured to (a) receive the collection cartridge and (b) decouple the sample tray from a housing of the collection cartridge.

An environmentally enhanced pipette tip rack includes a molded fibrous cellulose shell and an injection molded plastic tip deck; the shell and other features of the rack are configured for strength, minimal contamination, and to be biodegradable, compostable, or recyclable.

Provided herein is an integrated sampling and testing device, comprising a sampling device that comprises a syringe and specimen collector, and a testing device that comprises a cap, cylindrical container, and adaptor configured for sampling or testing.

Air-matrix digital microfluidics (DMF) apparatuses and methods of using them to prevent or limit evaporation and surface fouling of the DMF apparatus. In particular, described herein are air-matrix DMF apparatuses and methods of using them including thermally controllable regions with a wax material that may be used to selectively encapsulate a reaction droplet in the air gap of the apparatus; additional aqueous droplets may be combined with the encapsulated droplet even after separating from the wax, despite residual wax coating, by merging with an aqueous droplet having a coating of a secondary material (e.g., an oil or other hydrophobic material) that may remove the wax from the droplet and/or allow combining of the droplets.

Methods, systems and related compositions are provided to perform single-cell marking of a nucleic acid and/or protein in a sample based on in-cell or in-organelle barcoding of nucleic acid and/or protein complexes of the cell or organelle; the methods and systems herein described are configured to provide in-cell or in-organelle single-cell marked nucleic acid and/or protein complexes comprising a single-cell, cell-specific, or a single-cell organelle-specific marker.

An apparatus includes a flow cell body, a plurality of electrodes, an imaging assembly, and one or more barrier features. The flow cell body defines one or more flow channels and a plurality of wells defined as recesses in the floor of each flow channel. Each well is fluidically coupled with the corresponding flow channel. The flow cell body further defines interstitial surfaces between adjacent wells. Each well defines a corresponding depth. Each electrode is positioned in a corresponding well of the plurality of wells. The electrodes are to effect writing of polynucleotides in the wells. The imaging assembly is to capture images of polynucleotides written in the wells. The one or more barrier features are positioned in the wells, between the wells, or above the wells. The one or more barrier features contain reactions in each well, reduce diffusion between the wells, or reduce optical cross-talk between the wells.

An apparatus for testing a fluid sample including a sample receiving member having an opening for receiving a fluid sample, wherein the sample receiving member comprises at least a first and second sample collection chambers, a sample retention member, in fluid communication with the first sample collection chamber, to retain a portion of the fluid sample, and at least one test strip, in fluid communication with the second collection chamber, to indicate the presence or absence of at least one analyte in the fluid sample, wherein the first collection chamber is not in fluid communication with the second collection chamber.