An optical flow cell cuvette with short optical and fluidic paths, perpendicular to one another, with neither constriction nor any obstruction to fluid flow in the fluidic channel. Optical windows mounted flush to the walls of the rectangular fluidic channel keeps the light path short while keeping through-put high and maintaining a uniform cross-sectional area along the whole channel. Optical windows are independent of body structure allowing flexibility in manufacture and application.

A quantitative method for diagnosing an autoimmune disease or an infectious disease comprising performing an automated diagnostic assay, comprising: incubating a capture reagent with a streptavidin-coated medium to form a solid phase complex, wherein the capture reagent is a biotinylated autoantigen or infectious disease antigen; washing the solid phase complex to remove excess capture reagent; incubating the solid phase complex with a serum sample to form an immune complex; washing the immune complex to remove any unbound sample; incubating the immune complex with a conjugate to create an immune-conjugate complex; washing the immune-conjugate complex to remove any unbound conjugate; introducing a substrate capable of generating a quantifiable response; and calibrating the response generated from introducing the substrate.

Provided are a carbon isotope analysis device high in partial pressure of carbon dioxide isotope in gas sent into as optical resonator, and high in sensitivity performance and analytical accuracy, and an analysis method by use of the carbon isotope analysis device. A carbon isotope analysis device including a carbon dioxide isotope generator provided with a combustion unit that generates gas containing carbon dioxide isotope from carbon isotope, and a carbon dioxide isotope purifying unit; a spectrometer including an optical resonator having a pair of mirrors, and a photodetector that determines intensity of light transmitted from the optical resonator; a carbon dioxide trap including a cooler for freezing the carbon dioxide isotope, the carbon dioxide trap being disposed between the carbon dioxide isotope generator and the spectrometer; and a light generator.

An embodiment of a module system configured to interface with a microscope is described that comprises an input optical fiber configured to provide an excitation light beam from an external light source; dynamic alignment mirrors configured to adjust the position of the beams paths of the excitation light beam on a first plane; a coupling comprising a first end configured to engage with a complementary end, wherein the excitation light reflects off a turning mirror and travels along a beam path on a second plane through an orifice in the coupling; and an output optical fiber for delivering light from a sample to an external detector, wherein the light from the sample travels along the beam path on the second plane through the orifice in the coupling, reflects off the turning mirror and travels along one of the beam paths on the first plane to the output optical fiber.

A quantitative method for diagnosing an autoimmune disease or an infectious disease comprising performing an automated diagnostic assay, comprising: incubating a capture reagent with a streptavidin-coated medium to form a solid phase complex, wherein the capture reagent is a biotinylated autoantigen or infectious disease antigen; washing the solid phase complex to remove excess capture reagent; incubating the solid phase complex with a serum sample to form an immune complex; washing the immune complex to remove any unbound sample; incubating the immune complex with a conjugate to create an immune-conjugate complex; washing the immune-conjugate complex to remove any unbound conjugate; introducing a substrate capable of generating a quantifiable response; and calibrating the response generated from introducing the substrate.

A quantitative method for diagnosing an autoimmune disease or an infectious disease comprising performing an automated diagnostic assay, comprising: incubating a capture reagent with a streptavidin-coated medium to form a solid phase complex, wherein the capture reagent is a biotinylated autoantigen or infectious disease antigen; washing the solid phase complex to remove excess capture reagent; incubating the solid phase complex with a serum sample to form an immune complex; washing the immune complex to remove any unbound sample; incubating the immune complex with a conjugate to create an immune-conjugate complex; washing the immune-conjugate complex to remove any unbound conjugate; introducing a substrate capable of generating a quantifiable response; and calibrating the response generated from introducing the substrate.

A quantitative method for performing an automated diagnostic assay, comprising: incubating a capture reagent with a streptavidin-coated medium to form a solid phase complex; washing the solid phase complex to remove excess capture reagent; incubating the solid phase complex with a serum sample to form an immune complex; washing the immune complex to remove any unbound sample; incubating the immune complex with a conjugate to create an immune-conjugate complex; washing the immune-conjugate complex to remove any unbound conjugate; introducing a substrate capable of generating a quantifiable response; and calibrating the response generated from introducing the substrate.

Systems and methods are provided for determining a presence, type, or amount of an analyte in fluid. An analyte sensor can include a substrate that includes a chiral molecule for sensing the presence of the analyte in the fluid. A property of the chiral molecule may change in response to sensing the presence of the analyte. The change in the property of the chiral molecule can cause a change in polarization of a beam of light traveling through the substrate. The presence, type, or amount of the analyte can be determined based on the change in polarization of the beam of light. The analyte sensor, along with optical fibers, can be used to determine the presence, type, or amount of an analyte in a fluid sample from a wellbore.

A laser absorption spectroscopy exhaust gas sensor includes an optical cell with porous walls having pores with a mean diameter in the range of 0.1 nm to 1 mm; gold mirrors within the optical cell positioned to support a multi-pass optical path within the optical cell; an active heating element adapted to heat the optical cell to prevent condensation; a laser adapted to generate a laser beam; an optical detector adapted to detect a returning laser beam; and a processor for controlling the laser and the active heating element and for analyzing signals from the optical detector to identify a gas in the optical cell.

An apparatus for analyzing microbiome according to an embodiment of the inventive concept includes a light source unit configured to excite first light, a sample unit on which a sample to which the first light is incident is disposed, and a data analysis unit configured to receive second light emitted from the sample unit and analyze microbiome in the sample from the second light. Here, the sample unit includes a conductive polymer structure that surrounds the sample.