Abstract: A urine testing device and a smart toilet having the urine testing device, which includes a base, a paper feeding module, a sample adding module, and a testing module installed on the base and arranged in a linear form. The paper feeding module has a test paper box, a lifting mechanism, and a pushing mechanism. A horizontal paper leakage groove is disposed at a bottom of the test paper box to receive a bottommost piece of test paper. The lifting mechanism lifts and descends the test paper box to reveal/seal the paper leakage groove. The pushing mechanism pushes out test paper from the paper leakage groove and delivers test paper to the sample adding and testing modules. The sample adding module dropwise adds urine to be tested on test paper. The testing module tests test paper added with the sample to obtain a urine testing result.

Abstract: An automatic analyzer (100) includes: a storage unit (21b) that stores various parameters of the automatic analyzer (100) in association with each of elevations used in the automatic analyzers (100), the parameters being optimized for each of the elevations; an input unit (21d) that acquires information of an elevation at which the automatic analyzer (100) is provided; and a controller (21a) that reads the parameters stored in the storage unit (21b) and sets the read parameters to the automatic analyzer (100) based on the elevation acquired by the input unit (21d). As a result, various parameters can be easily adjusted according to a usage environment of the device.

Abstract: A system includes an optical measurement unit that measures an optical property of a whole blood sample deposited on a surface of a substrate, an ion source that causes ions derived from the whole blood sample, including ions formed from an analyte of interest present in the whole blood sample, to be emitted from the substrate, a mass analyzer that receives the ions emitted from the substrate and measures an abundance of at least one ion species corresponding to the analyte of interest, and at least one computing device that determines, based on the measured optical property, a hematocrit of the whole blood sample, and determines, based on the determined hematocrit of the whole blood sample and the measured abundance of the at least one ion species, a concentration of the analyte of interest per unit volume of blood plasma.

Abstract: An automatic analyzer allows identification of the patient specimen for which the specific reagent and the standard solution have been used, and verification of reliability of the analysis results. A plot mark 1-10 is determined depending on whether or not codes and lots as management information of the reagent, standard solution, and accuracy control sample are the same as those used last time. The plot 1-3 represents the start of using the reagent, and 1-4 the reagent use area. The plot 1-5 represents generation of calibration curve data from the standard solution and 1-6 a standard solution use area. The plot 1-7 represents measurement of the accuracy control sample and 1-8 an accuracy control sample use area from a time point of measuring the accuracy control sample as indicated by the plot 1-7 until the next time point. The measurement information 1-14 is the region for displaying the measurement results.

Abstract: A photonic chip has at least one input waveguide, at least one output waveguide, one of at least one Mach-Zehnder interferometer and at least one resonator, and a one-sided optical port enabling in and out coupling of light where the input waveguide begins and the output waveguide ends.

Abstract: A microfluidic bead-packing method includes activating a first micropump to transfer active microbeads through an inlet microchannel from a bead suspension reservoir to an adsorbing channel; packing the microbeads in the adsorbing channel; and activating a second micropump to reverse flow through at least a portion of the inlet microchannel and to transfer a sample fluid through the inlet microchannel from a sample reservoir to the adsorbing channel such that the sample fluid interacts with the packed microbeads.

Abstract: A laboratory sample distribution system is presented. The laboratory sample distribution system comprises an optical inspection device adapted to optically inspect items that need to be optically inspected, at least one mirror device, a driver adapted to move the items to be optically inspected and to move the at least one mirror device, and a control device configured to move an item to be optically inspected relative to the optical inspection device by controlling the driver such that a field of view of the optical inspection device is extended.

Abstract: A system for asservation of at least one hair including a hair root and a hair shaft are disclosed. In some embodiments, the system includes transport and/or storage containers, or cultivation containers. Also disclosed are methods for transporting and/or storing hair, for culturing keratinocytes from hair, and for generating induced pluripotent stem cells from keratinocytes.

Abstract: The present disclosure provides a consumable box automatic transmission device. The consumable box automatic transmission device includes a consumable box storage mechanism, configured to load and store consumable boxes, and a consumable box lifting mechanism, located above the consumable box storage mechanism; the consumable box lifting mechanism is able to lift the consumable boxes; the consumable box storage mechanism and the consumable box lifting mechanism is able to respectively store and transmit the consumable boxes; the consumable box storage mechanism is able to transmit the consumable boxes to the bottom of the consumable box lifting mechanism; and the consumable box lifting mechanism receives the consumable boxes at a bottom and lifts the consumable boxes to a top layer of the consumable box lifting mechanism. In this way, parallel consumable box transmission can be achieved, and continuous consumable box conveyance is achieved, thereby reducing manual care or frequent manual operation.

Abstract: A sample distribution system 1 has a regulator 4 for receiving a pipetting unit 2 that has at least one exchangeable pipette tip 3, wherein the regulator 4 is configured to change the position of the pipetting unit 2 in relation to a base plate 5, and to detect the presence or absence of pipette tips 3 with a sensor unit 12. According to the invention, the sensor unit 12 is a photoelectric sensor, in particular a reflection photoelectric sensor, with a detection range. The sensor unit 12 and the pipetting unit 2 can also move in relation to one another, in order to determine the presence of a pipette tip 3, if the pipette tip is in the detection range of the sensor unit 12.

Abstract: Provided is a method for developing biological trace evidence on a porous object, including immersing a porous object in a biological fluorescent development reagent or spraying the reagent on the porous object, drying the porous object in an environment having a relative humidity of less than 40% at a temperature of 50° C.-120° C. irradiating the dried porous object with a laser having a wavelength of 532 nm and a full width at half-maximum of less than 1 nm, controlling a surface of the porous object with an illuminance of over 300,000 lux, and using a cut-off filter under 540 nm to develop the biological trace evidence. A raw material formulation of the reagent is, in percent by weight, 0.02%-0.5% of indanedione, 4%-10% of ethyl acetate, 0.5%-1.5% of glycerol, 5%-15.5% of pure alcohol, and 73.5%-90% of petroleum ether.

Abstract: Disclosed is an automated liquid-phase immunoassay apparatus used with a cuvette having a plurality of chambers containing a reagent necessary for detection of an analyte in a biological specimen. The apparatus includes a movable cuvette module equipped with the cuvette, an optical reading module for optical assaying of a material resulting from a reaction between the specimen and the reagent, and a dispenser module which is positioned on the cuvette module and which dispenses the specimen and the reagent to the plurality of chambers of the cuvette and washes the specimen and the reagent therefrom.

Abstract: An embodiment provides a method for measuring amines in a solution, including: preparing an indicator-metal complex, wherein the indicator-metal complex comprises an indicator and a metal; introducing the indicator-metal complex to a solution, wherein the solution contains an amount of amine, wherein the amine activates the indicator-metal complex causing a change in fluorescence intensity of the indicator-metal complex; and measuring the amount of amine in the solution by measuring the change in fluorescence intensity of the indicator-metal complex.

Abstract: A biosensor for detecting the presence of a target compound in a test solution is disclosed. The biosensor includes upper and lower carrier plates, a spacer film with a micro-channel, an inlet port upstream of the micro-channel, an outlet port downstream of the micro-channel, a micro-machined transceiver, and a first molecularly imprinted polymer layer for recognizing and binding the target compound. The micro-machined transceiver includes a micro-machined transmitter for generating an acoustic wave, and micro-machined receiver for generating an acoustic wave-induced voltage. An amplitude of the acoustic wave-induced voltage is varied in response to the concentration of the target compound.

Abstract: Methods and systems for detecting and quantifying film forming amines in water systems are described. Water containing a film forming amine is combined with a fluorescent dye, the pH of the water is reduced, and then the fluorescence signal of the fluorescent dye is measured. The fluorescence signal is indicative of the amount of film forming amine in the water, and can be used to quantify the amount of film forming amine and control the amount of film forming amine that is introduced into the water system.

Abstract: There is provided an automated analyzer which can eliminate static charge on receptacles storing analytes or reagents to thereby offer improved accuracy of analysis. The automated analyzer comprises: a receptacle carrier mechanism operative to hold a plurality of receptacles storing liquid and to carry the held receptacles in a given direction; a reader device for reading identification information of the receptacles carried by the receptacle carrier mechanism; a static eliminator for eliminating static charge on the receptacles carried by the receptacle carrier mechanism; and an input/output controller for causing the static eliminator to carry out the elimination of the static charge in synchronism with successive reading by the reader device of the identification information of the receptacles carried by the receptacle carrier mechanism.

Abstract: An automatic analyzer capable of controlling an interval between the tip of a sample nozzle and the bottom of a reaction container regardless of individual differences between reaction containers and sample nozzles and suppressing adhesion of a sample to the sample nozzle is disclosed. Sample nozzles 13a and 14a are moved toward the bottom surface of a reaction container 2, the movement of the sample nozzles is stopped at a point in time when a stop position detector 46 detects a stop position detection plate 45, the sample nozzles are ascended from the stop position to a position where the stop position detection plate 45 separates from a detection range of the stop position detector 46, and an arm 44 is moved upward by a moving distance stored in a memory.

Abstract: Operability, accuracy, and safety when fitting a glass-made pipette tip to a pipette are improved. A pipette tip fitting adapter includes a hollow body having one end portion configured to serve as a tip inserting portion into which a pipette tip is inserted, and the other end portion configured to serve as a pipette inserting portion into which a pipette is inserted, and at an opening side of an inner circumferential surface of the tip inserting portion, seal portions projecting inward are formed in a circumferential direction. Accordingly, a pipette tip that is long and heavy like a glass tip can be held.