The present disclosure provides methods, systems, and kits for detecting molecules in a sample with a pre-equilibrium digital immunoassay. The methods and systems provide means for quantifying molecules in a biological sample of minimal volume in short amounts of time.

An electric meter for measuring metal impurities in a fuel tank, comprising: a frame; two electric electrodes supported by the frame; an electric measurement meter connected to the two electric electrodes by using two conductive wires; the electric measurement meter serving to measure the electric properties between the two electric electrodes. In use, the frame with the two electric electrodes is placed into a fuel tank and is sunk into the bottom of the fuel tank; and the electric force of the two electric electrodes will attract the metal impurities in the fuel tank so that the electric measurement meter can measure the electric properties between the two electric electrodes; by the electric property, it can be used to determine the quantity of the metal impurities within the fuel tank so as to determine whether the fuel tank exists too much metal impurities and is needed to be cleaned.

A system for detecting microbes is provided. In the system for detecting microbes, light is emitted to a sample through a light emission module, a sensor module detects speckles generated when the emitted light is scattered by motion of bacteria or microbes contained in the sample, and a controller stores and analyzes images detected by the sensor module to test microbial detection, wherein controller may include a light emission controller connected to the light emission module and configured to control an emission period and an emission intensity of light emitted by the light emission module; an imaging collector connected to the sensor module and configured to store a speckle image generated through multiple scattering by the bacteria or microbes contained in the sample; a corrector configured to correct a deviation caused by a difference in the amount of light when the light emission module emits the light; and an estimator configured to estimate, in real-time, presence or absences of the bacteria or microbes in the sample or a concentration of the bacteria or microbes.

According to an embodiment of the disclosure, a device for measuring a turbidity of a solution containing fine particles comprises a laser module emitting a laser beam of a predetermined wavelength band, a coupler outputting the laser beam along a first laser path and a second laser path divided from each other, a probe outputting the laser beam output along the first laser path to a container containing the solution, a light receiving element receiving, through the first laser path, the laser beam reflected or scattered by the fine particles in the solution and detecting the received laser beam, and a controller calculating the turbidity based on a strength of the laser beam detected by the light receiving element.

Cell counting device A cell counting device and a method of using a cell counting device are disclosed. The cell counting device comprises a chamber for receiving a sample, at least one light source to emit light towards a section of the chamber. The section of the chamber comprises a sub-sample of the sample. The cell counting device also comprises a light detector to receive a light emitted from the section of the chamber and to generate an electronic signal associated with the received light, and a controller. The controller is configured to estimate the number of photoactive cells in the sample by calculating the distribution of variable fluorescence [F.sub.v] values of a predetermined number of sub-samples about the mean F.sub.v value.

A nebulizer system capable of identifying when activation has occurred and aerosol is being produced. The nebulizer system monitors the inhalation and exhalation flow generated by the patient and communicates proper breathing technique for optimal drug delivery. The nebulizer system may monitor air supply to the nebulizer to ensure it is within the working range and is producing, or is capable of producing, acceptable particle size and drug output rate. When a patient, caregiver or other user deposits or inserts medication into the nebulizer, the nebulizer system is able to identify the medication and determine the appropriate delivery methods required to properly administer the medication as well as output this information into a treatment log to ensure the patient is taking the proper medications. The system is able to measure the concentration of the medication and volume of the medication placed within the medication receptacle, e.g., bowl.

A method for evaluating a biological material for unassociated virus-size particles having a particular epitope uses a fluorescent antibody stain specific for binding with the epitope and a fluid sample with the virus-size particles and fluorescent antibody stain is subjected to flow cytometry with identification of fluorescent emission detection events indicative of passage through a flow cell of a flow cytometer of unassociated labeled particles of virus size including such a virus-size particle and fluorescent antibody stain.

A cell detector and a cell detection method detect cell proliferation. A cell detector includes a light emitter, a culture vessel that accommodates a culture medium containing a cell, a first slit member including a first slit and a first light shield, and at least one light receiver that receives light emitted from the light emitter and passing through the culture medium and the first slit in the first slit member in an order of the culture medium and the first slit. The first light shield in the first slit member blocks light emitted from the light emitter and scattered by the cell in the culture vessel when the cell is at a position overlapping the first slit.

Devices and methods for measuring analytes and target particles in a sample are disclosed. In some embodiments, the disclosure provides a cartridge device. In other embodiments, the disclosure provides a method of using a cartridge device as disclosed herein for analyzing analytes and target particles in a sample. In further embodiments, the disclosure provides an analyzer including a cartridge device and a control unit device. The control unit device is configured to receive, operate, and/or actuate the cartridge device. In some embodiments, the disclosure provides a method of using an analyzer as disclosed herein for analyzing analytes and target particles in a sample.

A method for calibrating a contaminant detection device includes fluidly connecting the contaminant detection device in series to a test reservoir and a light-obscuration-type particle counter, pumping low-end, intermediate, and high-end test dust dilutions through the contaminant detection device and the particle counter until a particle count measured by the particle counter for each of the successive test dust dilutions stabilizes, and setting a low-end gain, an intermediate gain, and a high-end gain for the contaminant detection device based on the stabilized particle counts for each of the test dust dilutions using a first-sized test dust grade. A bubble counting gain of an aeration threshold for the device may be set according to a second test dust grade greater in size than the first-sized test dust grade, and associated with a voltage signal produced by the contaminate detection device indicative of the presence of an air bubble contained within the fluid during use of the fluid in heavy machinery.