Abstract: The present disclosure relates to a method for manufacturing a test strip for multiplex immunoassay analysis and the test strip manufactured using same.

Abstract: Provided is a lateral flow assay device capable of detecting a traumatic brain injury marker including a sample pad into which a blood sample containing a traumatic brain injury marker is injected, an adsorption pad including a probe which is mixed to the marker when the traumatic brain injury marker moves from the sample pad to form a traumatic brain injury marker complex, and a porous film which fluid-communicates with the adsorption pad and capillary-migrates the traumatic brain injury marker complex from the adsorption pad to a detection line, in which the probe includes a capture antibody consisting of an antibody labeled with a specific binding material specifically binding to the traumatic brain injury marker and a detector antibody consisting of an antibody labeled with a fluorescent material having a relatively long emission lifetime of 1 microsecond or more, and a mixture of at least two different kinds-origin antibodies is used as the antibody labeled with the specific binding material or the fluor

Abstract: A fluid analysis cartridge having an improved structure in order to increase test reliability, and a fluid analysis apparatus including the same are disclosed.

Abstract: A sample analysis cartridge and a sample analysis apparatus having the sample analysis cartridge are provided. The sample analysis cartridge includes a housing having a sample injecting hole and a strip coupled with the housing such that a sample that is passed through the sample injecting hole is directed into the strip, and the strip is configured to detect a target material from the sample through an antigen-antibody reaction. The strip includes a membrane including a test line and a transparent cover disposed outside the membrane.

Abstract: A testing apparatus and control method thereof are provided.

Abstract: A fluid analysis cartridge having an improved structure in order to increase test reliability, and a fluid analysis apparatus including the same are disclosed.

Abstract: A fluid analysis cartridge includes a reference well including a macromolecular coloring reagent having an optical characteristic that varies according to a thickness of the reference well, and a test well including a test reagent having an optical characteristic that varies according to a concentration of a component of a fluid sample that reacts with the test reagent and a thickness of the test well.

Abstract: An electronic apparatus and an ultraviolet avoidance information providing method are provided. The electronic apparatus includes a display; a biometric information acquisition module that acquires biometric information of a user; a location information acquisition module that acquires location information of a particular location; an ultraviolet intensity information acquisition module that acquires ultraviolet intensity information corresponding to the acquired location information; and a processor that controls the display to display ultraviolet avoidance information for avoiding ultraviolet light at the particular location based on the acquired biometric information and the acquired ultraviolet intensity information.

Abstract: A specimen analysis apparatus and measurement method thereof are provided. The specimen analysis apparatus includes: a cartridge including at least two containers, at least one of the at least two containers containing an internal standard material including a target material; and a controller configured to determine a correction value for a concentration of the target material by comparing an extent of a change in optical signal values of the target material measured in the at least two containers with a predetermined extent of change in the optical signal values of the target material..

Abstract: A fluid analysis cartridge includes a reference well including a macromolecular coloring reagent having an optical characteristic that varies according to a thickness of the reference well, and a test well including a test reagent having an optical characteristic that varies according to a concentration of a component of a fluid sample that reacts with the test reagent and a thickness of the test well.

Abstract: A method for amplifying a nucleic acid amplification in the presence of an ionic liquid that suppresses an inhibitor of nucleic acid amplification, particularly when in a biological material, and a composition useful for performing the method.

Abstract: An electronic device and method that detects an event related to the user's skin and performs a function corresponding to the event by using information on the skin color type of the user, and further provides a control method thereof. The occurrence of an event is detected that is related to at least a part of a user's body. Information regarding a light is obtained a sensor module that is functionally connected with the electronic device according to the detection result. A function is performed that corresponds to the detected event by using information corresponding to the obtained information on a light from among type information stored in a memory.

Abstract: A method of detecting a target nucleic acid, and a polynucleotide and a composition for detecting a target nucleic acid.

Abstract: An electronic apparatus and an ultraviolet avoidance information providing method are provided. The electronic apparatus includes a display; a biometric information acquisition module that acquires biometric information of a user; a location information acquisition module that acquires location information of a particular location; an ultraviolet intensity information acquisition module that acquires ultraviolet intensity information corresponding to the acquired location information; and a processor that controls the display to display ultraviolet avoidance information for avoiding ultraviolet light at the particular location based on the acquired biometric information and the acquired ultraviolet intensity information.

Abstract: A polynucleotide comprising a first region the 5? end of which is complementary to a portion of a target nucleic acid, a cleavable second region, a third region having a stem-loop structure, and a fourth region complementary to the 3? end of the first region, and use of the polynucleotide, as well as a composition comprising two such polynucleotides each of which hybridize different strands of a double-stranded target nucleic acid, and methods and kits using the same for amplifying targets.

Abstract: Provided is a reagent container that can maintain stability of a reagent for a long period of time, a method of preparing the reagent container, a method of storing the reagent, and microfluidic systems for conducting cell binding, lysis, nucleic acid extraction, and amplification.

Abstract: An efficient method of processing a target material in a sample using a microfluidic device including an elastic membrane.

Abstract: A composition and kit for detecting Clostridium difficile including a primer set for detecting a strain of Clostridium difficile, and a method of detecting Clostridium difficile by using the same.

Abstract: A gene analysis apparatus includes a sample preparation chip in which a polymerase chain reaction (“PCR”) sample is prepared, a PCR chip in which a PCR is performed on the PCR sample, and a package layer on which the sample preparation chip and the PCR chip are mounted. The package layer includes a channel through which a material flows from the sample preparation chip to the PCR chip. The sample preparation chip and the PCR chip are on a same side or on opposing sides of the package layer.

Abstract: A method of lysing at least one of a cell and a virus, the method including: contacting a sample, which includes at least one of a cell and a virus, with a plurality of beads which are disposed in a first chamber to obtain a combination of the sample and the beads; and agitating the combination of the sample and the beads to lyse the at least one of the cell and the virus, wherein in the first chamber a liquid volume fraction is 0.6 or less, and wherein the liquid volume fraction is a value obtained by dividing a liquid volume of the first chamber by a pure void volume equivalent to a sum of the liquid volume of the first chamber and a void volume of the first chamber.