A method of multispectral immunofluorescence imaging of a biological sample is described. The described method allows direct detection of seven or more target antigens simultaneously using directly labeled antibody fluorophore conjugates. The described method enables multiplex detection and analysis of a plurality of biomarkers simultaneously across an entire planar biological sample, providing unique spatio-temporal insights in immune-therapeutics and immuno-diagnostics.

To provide a microscope device capable of efficiently or appropriately acquiring an image of a specific region of a living tissue.

The present technology provides a microscope device including: a first imaging element that images a target including a body tissue and acquires image data; and a second imaging element that images the target at a magnification different from a magnification of the first imaging element and acquires image data, in which the first imaging element includes a determination unit that determines a feature related to the target on the basis of the image data, and the second imaging element is controlled on the basis of a result of the determination. Furthermore, the present technology also provides an image acquisition system including the microscope device. Furthermore, the present technology also provides an image acquisition method performed in the microscope device.

The disclosed technology relates to systems and methods for nucleic acid sequencing utilizing a single light source and a single detector. The disclosed technology may use the light source to stimulate a fluorescence emission from a polynucleotide and identify a nucleobase in the polynucleotide based on the intensity of the fluorescence emission received by the detector. The disclosed technology may utilize four types of nucleotide analogs which emit light at four distinguishable levels when excited by the light source. In various embodiments, the four types of nucleotide analogs may be coupled to different fluorophores or the same fluorophore with different probabilities or copy numbers.

An optical imaging system (1) is configured for photographing a sample and includes a lighting module (11) and an imaging module (15). The lighting module (11) is configured for outputting excitation light, the excitation light is configured to excite the sample to generate excited light, the imaging module (15) comprises a time delay integration line scan camera (151), the time delay integration line scan camera (151) is configured to record the excited light. A biochemical substance detection system using the optical imaging system (1) is also provided, improving the detection flux.

A main object of the present technology is to provide a technology for automatically presenting a better combination of fluorescent markers. The present technology provides an information processing system including an information processing device that includes a calculation processing unit that calculates an objective function regarding a combination of a biomolecule, the biomolecule being a labeling target in a sample, with a labeling phosphor, on the basis of first data listing information on the biomolecule, and second data listing information on the labeling phosphor, and an assignment information output unit that outputs information on assignment of the labeling phosphors to respective biomolecules, the information being generated on the basis of combination information acquired from a combinatorial optimization processing unit on the basis of a coefficient of the objective function.

A portable incubator system integrated to a mobile phone providing a real-time tracking of samples and data flow is provided. The portable incubator system allowing cells to be cultured, reproduced and characterized in real-time without a need for a commercial incubator and a microscope-camera system installed within the portable incubator system.

A device for the in-ovo determination of the sex of a fertilized bird egg, having a light source for emitting excitation radiation for exciting fluorescence in a region inside the bird egg, a spectroscopic apparatus for analysing, in a temporally and/or spectrally-resolved manner, fluorescence radiation emitted from the region inside the bird egg, an evaluation unit for determining the sex from the data determined by means of the spectro-scopic apparatus and a measuring head for jointly transmitting the excitation radiation into the bird egg and receiving the fluorescence radiation from the bird egg. The measuring head has an optical fibre system with a head end for transmitting the excitation radiation and receiving the fluorescence radiation.

The present invention relates to a rapid method for the direct quantification of Aflatoxin M1 (AFM1) in a sample of milk. The invention also relates to a device and the use thereof in implementing said method.

A fluorescence microscope, includes an optical system configured to collect fluorescent light emitted from different fluorophore species within a field of view and to focus the fluorescent light for detection, a spectral splitting arrangement configured to split the fluorescent light into at least two spectrally different fluorescent light components, a multi-channel detector system including at least two image sensors configured to detect at least two spatial light intensity distributions based on the at least two spectrally different fluorescent light components, each spatial light intensity distribution representing an image of the object over the field of view, and a processor configured to determine spatial distributions of the different fluorophore species based on a spectral unmixing analysis of each spatial light intensity distribution, wherein the processor is further configured to obtain compensation information and to determine a spatial distribution of each fluorophore species by taking into account the compensation information.

Disclosed herein are certain sets of antibody-fluorophore pairs comprising antibodies that specifically bind target antigens, the sets of antibody-fluorophore pairs thereby allowing visualization and quantification of a plurality of target antigens in a biological sample using multispectral tissue slide scanners. Also disclosed herein are methods of using such antibody-fluorophore pairs, and reagents related thereto.