A bilirubin assay system comprises a test card with a bilirubin test strip upon which a blood sample has been deposited, the bilirubin test strip comprising plasma from the blood sample. The bilirubin assay system further includes a mobile device with a camera, configured to capture an image of the test card that comprises the plasma on the bilirubin test strip and the set of calibration images. The system determines first and second calibration images, the first and the second calibration images having saturation values closest to a saturation value of the plasma on the bilirubin test strip. The system further determines a bilirubin level of the plasma on the bilirubin test strip based at least in part on interpolating a first color distance between the first calibration image and the plasma and a second color distance between the second calibration image and the plasma.

A test strip and analytical apparatus have pin connections permitting the definition of geographic regions or of particular customers. A test strip made for use in a particular region or for a particular customer will have pin connections matching features of the apparatus made for use in that region or by that customer. Insertion of the strip into the apparatus does not merely turn on the apparatus, but provides the regional or customer coding. Analog switches within the apparatus allow coding of a larger number of distinct regions or customers than would otherwise be possible, all without degrading the quality of the measurements made of the fluid being tested. Conductive paths in the strips permit testing the strips during manufacture so as to detect quality lapses regarding the printing or deposition of the paths.

An operation method of a multiplex slide plate device is provided. First, the multiplex slide plate device is assembled, including a slide plate, a sacrificial layer and a housing. The slide plate has reaction vessels, and the sacrificial layer has a microfluidic channel composed of an injection channel, a main channel and a distal channel. A sample solution is injected to the injection channel, such that the sample solution flows from the injection channel through the main channel to the distal channel, wherein the sample solution loads into the reaction vessels. Afterwards, an oil is injected to the injection channel, such that the oil flows from the injection channel through the main channel to the distal channel, wherein the oil removes the sample solution not loaded into the reaction vessels. Next, the sacrificial layer is heated to melt, and the melted sacrificial layer is mixed with the oil.

Provided are devices, systems and methods for evaluation of hemostasis. Also provided are sound focusing assemblies.

A microfluidic device includes an integrated circuit and a first substrate layer having a first surface and a second surface. The first surface of the first substrate layer is connected to the integrated circuit. The first substrate layer is in fluid communication with the integrated circuit. The microfluidic device also includes a second substrate layer having a surface area substantially larger than that of the first substrate layer. The second substrate layer includes a first and second surface. The first surface of the second substrate layer is connected to the second surface of the first substrate layer. The second substrate layer includes a first fluid inlet. The second substrate layer is in fluid communication with the integrated circuit through the first substrate layer.

An assembly for storing sample processing consumables can include a cover and a tray. The cover defines a cover cavity. The tray defines a first plurality of wells. The tray includes a first portion received within the cover cavity such that a press fit is formed between a first tray surface of the first portion of the tray and a first cover surface of the cover defining the cover cavity, thereby releasably coupling the cover to the tray. Each of the first plurality of wells contains a sample processing consumable. The assembly can be used to load sample processing consumables into a sample processing instrument.

A mobile, self contained molecular diagnostics system is provided with a microfluidic chip, detection apparatus and an integrated or wireless control interface and imager. The system provides automated sample preparation and rapid optical detection of multianalyte nucleic acids and proteins. On chip PCR may be performed to improve the optical fluorescence signal for nucleic acid detections. Plasmonic protein detection is performed using a dark field smartphone microscope. Dark field illumination is based on an evanescent field generated by LED total internal reflection. The smartphone element may also be used as an interface to control the detection apparatus, acquire images, process data and for wireless communications with remote computers. The handheld automated system has low power requirements and is particularly suited for point of care and on demand diagnostics in resource limited settings.

A manually-operated mono-channel or multi-channel pipette for the sampling and dispensing of a liquid sample in accordance with a given protocol, comprising a control button equipped with an autonomous control device which can supply a user with information relating to a pipetting operation in real time during the pipetting operation.

The disclosed subject matter provides a microdevice and techniques for single-cell gene expression profiling using a microfluidic device capable of cell-trapping, cell lysis, bead-based gene analysis. The microdevice can be capable of independent or parallelized, simultaneous quantitative genetic assays of single cells.

A fluid sample collection card in one embodiment includes an absorbent strip including a sample application portion, a first absorbent strip portion extending directly from the sample application portion, and a second absorbent strip portion extending directly from the sample application portion and spaced apart from the first absorbent strip portion by the sample application portion, a non-absorbent layer positioned beneath the absorbent strip, and a sample application portion indicium configured to identify the sample application portion.