A kit or set including a planar sample carrier having an absorbent membrane layer suitable for absorbing liquid blood components is provided, and wherein at least a portion of the blood components is able to dry in the membrane layer, wherein the sample carrier is additionally provided on an outer side with an optically readable code, additionally including a closable cuboidal box having a bottom surface that has a rectangular base surface and that additionally has a first opening, additionally including a planar receiving element having a base surface that corresponds to the base surface of the bottom surface, wherein the receiving element has a second opening and a holder that together are designed such that, on mounting the sample carrier in the holder and subsequently inserting the receiving element into the box on the bottom surface of the box, the optical code is visible through the first opening in the bottom surface and also through the second opening in the receiving element.

A stack of fluidics layers of a microfluidic cartridge for sequencing nucleic acid molecules includes a sequencing chamber layer having a sequencing chamber area configured for carrying out clustering and sequencing reactions, and a sequencing chamber bottom layer disposed under the sequencing chamber layer. The sequencing chamber bottom layer has an opening configured to hold an image sensor with the image sensor having an active area disposed under the sequencing chamber area. The sequencing chamber area spans substantially all of the active area of the image sensor. The stack of fluidics layers includes a flexible printed circuit board (PCB) layer under the sequencing chamber bottom layer, and a fluidics channels layer disposed under the flexible PCB layer. The fluidics channels layer includes fluidics channels that are configured to deliver reactants to the sequencing chamber area. The fluidics channels do not substantially overlap with the active area of the image sensor.

The present invention relates to sample analysis cartridges comprising micro-environment sensors and methods for assaying coagulation in a fluid sample applied to the micro-environment sensors, and in particular, to performing coagulation assays using micro-environment sensors in a point of care sample analysis cartridge. For example, the present invention may be directed to a sample analysis cartridge including an inlet chamber configured to receive a biological sample, and a conduit fluidically connected to the inlet chamber and configured to receive the biological sample from the inlet chamber. The conduit may include a micro-environment prothrombin time (PT) sensor, and a micro-environment activated partial thromboplastin time (aPTT) sensor.

In one example in accordance with the present disclosure, a cellular analytic system is described. The cellular analytic system includes an analytic device. The analytic device includes a chamber to receive a cell to be analyzed. At least one lysing element agitates the cell and at least one sensor detects a change in the cell based on an agitation of the cell. The cellular analytic system also includes a controller to determine a rupture threshold of the cell based on parameters of the agitation when a cell membrane ruptures.

A microfluidic cartridge, configured to facilitate processing and detection of nucleic acids, comprising: a top layer comprising a set of cartridge-aligning indentations, a set of sample port-reagent port pairs, a shared fluid port, a vent region, a heating region, and a set of detection chambers; an intermediate substrate, coupled to the top layer comprising a waste chamber; an elastomeric layer, partially situated on the intermediate substrate; and a set of fluidic pathways, each formed by at least a portion of the top layer and a portion of the elastomeric layer, wherein each fluidic pathway is fluidically coupled to a sample port-reagent port pair, the shared fluid port, and a detection chamber, comprises a turnabout portion passing through the heating region, and is configured to be occluded upon deformation of the elastomeric layer, to transfer a waste fluid to the waste chamber, and to pass through the vent region.

An assembly for storing sample processing consumables that includes a cover and a tray. The cover includes a flexible panel and a cover wall that extends downward from the perimeter of the panel, where the panel and the cover wall define a cavity. The tray has a top surface that defines a plurality of wells and a side surface that extends downward from the perimeter of the top surface. The panel is situated adjacent the top surface of the tray, where a first portion of the tray is received within the cover cavity, such that a press fit is formed between the side surface of the tray and an inner surface of the cover wall, thereby releasably coupling the cover to the tray. At least a portion of the wells contain a sample processing consumable, and the cover is configured to be decoupled from the tray by applying a force to the panel to overcome the press fit.

Devices and methods are provided for electrically lysing cells and releasing macromolecules from the cells. A microfluidic device is provided that includes a planar channel having a thickness on a submillimeter scale, and including electrodes on its upper and lower inner surfaces. After filling the channel with a liquid, such that the channel contains cells within the liquid, a series of voltage pulses of alternating polarity are applied between the channel electrodes, where the amplitude of the voltage pulses and a pulse width of the voltage pulses are effective for causing irreversible electroporation of the cells. The channel is configured to possess thermal properties such that the application of the voltage produces a rapid temperature rise as a result of Joule heating for releasing the macromolecules from the electroplated cells. The channel may also include an internal filter for capturing and concentrating the cells prior to electrical processing.

The present invention provides a test barrel for placing a test paper card. The test barrel comprises a barrel body and a barrel lid; wherein the barrel body comprises a place reminding board arranged on the barrel body; and the barrel lid comprises an elastic piece arranged on the barrel lid and mating with the place reminding board. The test barrel for placing a test paper card according to the present invention is simple in structure and convenient in operation, and greatly reduces time for test. In addition, a place reminding structure is arranged on the test barrel, which facilitates use of the test barrel for the user and achieves sealing reminding. Further, the test result is accurate, the reusage rate is high, and cleaning is convenient.

Disclosed is a real-time method for detecting copper and silver in water in parts per billion. Total silver is detected by adding a nitric acid solution to the sample; after the silver is digested, adding a buffer solution comprising water, sodium bicarbonate, sodium carbonate and EDTA to the sample; adding an indicator comprising Cadion 2B, EtOH, and Triton X-100 to the sample; then reading the absorbance of the sample after light with an approximate target peak of 515 nm is sent through the sample; and determining the silver concentration by comparing the absorbance of the sample to the absorbances of known silver standards. Total copper is detected by adding a nitric acid solution to the sample; after the copper is digested, adding a buffer/indicator solution to the sample, where the solution comprises water, sodium citrate dihydrate, hydroxal amine hydrochloride and bathocuproine disulfonate; after one minute, reading the absorbance of the sample after light with an approximate target peak of 480 nm is sent through the sample; and determining the copper concentration by comparing the absorbance of the sample to the absorbances of known copper standards. A monitoring device for determining the level of copper or silver in a sample implements the disclosed methods.

An apparatus includes a plate and a microheater. The plate defines a sample reservoir, component reservoirs, an outlet, a microfluidic channel, and branches. The sample reservoir is configured to hold a specified sample volume of a hydrocarbon sample. Each component reservoir is configured to hold a respective specified component volume of a different one of the hydrocarbons. The microfluidic channel extends from the sample reservoir to the outlet. Each branch connects a different one of the component reservoirs to the microfluidic channel. The microheater is an electrical resistor that is configured to provide heat to the hydrocarbon sample held in the sample reservoir. The hydrocarbon sample fractionates into the hydrocarbons, which are distributed across the component reservoirs, as the hydrocarbon sample flows from the sample reservoir to the outlet in response to receiving the heat from the microheater.