The present invention provides a wide-area sample-based reader design which serves as a diagnostic detection device for bio-particles.

Provided herein are methods for preparing biological samples for spatial proteomic analysis, methods of determining a location of a protein analyte in a biological sample, and methods of determining a location of a protein analyte and a nucleic acid analyte in a biological sample.

A device for exciting objects with an excitation radiation and for detecting a photoluminescence radiation emitted by the objects after the absorption of the excitation radiation. The device includes a wall in contact with the objects, an organic light-emitting diode for emitting the excitation radiation and transparent to the photoluminescence radiation, an optical resonator tuned to the wavelength of the photoluminescence radiation and located on the side of the organic light-emitting diode opposite to the wall, and at least one sensor of the photoluminescence radiation arranged on the side of the optical resonator opposite to the organic light-emitting diode.

In-situ fluorimeters and methods and systems for collecting and analyzing sensor data to predict water source contamination are provided. In one embodiment, a method is provided that includes receiving sensor data regarding a water source. Changepoints may then be calculated within the sensor data and the sensor data may be split into intervals at the changepoints. A machine learning model may then be used to classify the intervals and a predicted contamination event for the water source may be identified based on the classified intervals. In another embodiment, an in-situ fluorimeter is provided. The in-situ fluorimeter comprises one or more UV LEDs centered around a pre-set excitation wavelength (e.g., a TLF excitation wavelength), a bandpass filter, a lens, a photodiode system, a machine learning platform; and an alarm triggered by contamination events, wherein the alarm is calibrated through the machine learning system.

A miniaturized chromatographic inspection apparatus capable of optimal light emission and reading control according to the type of marker, and a control method thereof. The apparatus can comprise: a main body; a cartridge tray with a seated immunochromatographic test cartridge, configured to be accommodated in the main body or to be withdrawn to the outside of the main body; a tray driving unit for moving the cartridge tray; an image sensing unit for recognizing a code expression provided on a surface of the cartridge or excitation light generated from the cartridge; a first light source illuminating the code expression provided on the surface of the cartridge; a second light source illuminating a window of the cartridge to generate the excitation light in the cartridge; and a control unit for controlling the tray driving unit, the first and second light source, and processing information acquired from the image sensing unit.

A chromatographic testing device which is configured to select an imaging scheme according to the type of fluorescent dye in an immunochromatographic test cartridge and a method for controlling the same are disclosed. The chromatographic testing device can include: a body; a code expression recognition unit provided in the body and recognizing a code expression in which a type of fluorescent dye of an immune strip provided on an immunochromatographic test cartridge mounted on the body is recorded; an excitation light source emission unit for emitting light from an excitation light source to the immunochromatographic test cartridge; an image sensor unit for recognizing excitation light generated by the excitation light source; and a control unit for controlling the image sensor unit in a single imaging scheme or a cumulative light imaging scheme according to the type of fluorescent dye of an immune strip, recognized by the code expression recognition unit.

An inspection system for optical surface inspection of a test specimen having a fluorescent agent arranged on the test specimen includes an illumination system, an optical detection system, and a detection filer system. The illumination system is for illuminating the test specimen and the fluorescent agent with illuminating radiation, and includes one or more illuminating means. The optical detection system is for detecting fluorescent radiation emitted by the test specimen with the fluorescent agent. The detection filter system is set up to filter illumination radiation of the illumination system in the inspection system in such a way that the optical detection system only detects fluorescence radiation from the fluorescence agent.

The present invention provides methods and systems for encoding and decoding of synthesis steps and conditions of combinatorial synthesis of molecular library on carrier-beads. The encoding is performed at each step of synthesis by attachment of smaller fluorescently labelled beads (label-beads) to the surface of a carrier-bead (carrier-bead). The number of label-beads should be such that each is spatially resolvable on a surface of the carrier-bead. Alternatively label-beads are detachable, or the carrier-bead are dissolvable, so the label-beads could be dispersed over large enough distance to be resolved spatially. The fluorescent spectrum of each of the label-beads carries information of the synthesis step and synthesis, i.e., a spectral barcode or binary encoding system. During decoding of the spectrally identified label-beads, a fluorescent spectrum of each spatially resolvable label-bead is determined.

A device includes a plurality of imaging pixels in a spatial pattern with a formation of features disposed over the pixels. A first and a second feature of the formation of features are disposed over a first pixel. A first luminophore is disposed within or over the first feature. A second luminophore is disposed within or over the second feature. A structured illumination source is to direct at least a portion of first photons in an illumination pattern to the first feature at a first time, and to direct at least a portion of second photons in the illumination pattern to the second feature at a second time. The structured illumination source includes an illumination pattern generator having an illumination pattern generator actuator connected to the illumination pattern generator to cause the illumination pattern to translate or rotate relative to the formation of features.

Hardware and control software for use in the field of digital imaging and spectroscopy. More particularly, a hardware and software system that simultaneously measures electromagnetic energy as quantities of photons in distinct wavelength regions across the ultraviolet, visible, and infrared spectrum. The system records the measurements as digital data and employs a processor (preferably a programmable processor) that executes processing steps to enhance the spatial and spectral fidelity of the recorded signals. More specifically, the electro-optical sensor hardware is engineered to maximize the light collection efficiency, especially for low light intensities, by using multiple detectors, each of which is optimized individually to maximize its sensitivity to specific wavelength regions of interest. The detector system also employs a variable amplification process that is dependent on the signal intensity so that low signals can be increased for better detection while high signals are amplified less to stay within the dynamic range of the optical sensor that is used to convert the analog signal to a digital value. Solutions to existing problems of low light detection are provided as are new capabilities for data collection and analysis in previously undetectable low signal regimes. The systems and methods are applicable to a broad array of imaging applications in diverse fields from biomedical imaging to astronomy and remote sensing.