Abstract: There is provided a calculation method of calculating a starting point (Xs, Ys) of signal rise from a fluorescence signal measured using a biological sample, wherein the fluorescence signal is time-series data including a dataset (measurement time, fluorescence intensity) of the fluorescence intensity for the measurement time and wherein the calculation method includes a process of calculating a temporary starting point (Xs?, Ys?) and a process of calculating the starting point (Xs, Ys) of the signal rise on the basis of the temporary starting point (Xs?, Ys?).

Abstract: The present invention relates to a method for evaluating phagocytic capacity of phagocytes, including incorporating a fluorescent substance into phagocytes in a sample containing whole blood to obtain a measurement sample, standing the measurement sample for 2 minutes or more, measuring the fluorescence of the fluorescent substance, and evaluating the phagocytic capacity of phagocytes based on the intensity of the measured fluorescence, in which the measuring the fluorescence of the fluorescent substance includes irradiating an intermediate region of gravity direction of a placed measurement sample with an excitation light, and detecting the fluorescence generated from the fluorescent substance by the excitation light.

Abstract: Provided is a measurement container including a container body where a first region, a second region, and an intermediate region are continuously formed as an accommodation space accommodating a sample and an inlet is formed and a rotor which is arranged in the second region and rotated by an effect of magnetic force. The container body includes a wall portion which defines the accommodation space and at least a portion of which has a light transmitting property and a partitioning portion which partitions the intermediate region into one side and the other side in a second direction perpendicular to the first direction. The partitioning portion partitions the intermediate region into the one side and the other side so that a communication region which allows the one side and the other side to communicate with each other in the intermediate region remains.

Abstract: To provide a pathological index for Alzheimer's disease conveniently and with high precision, an Alzheimer's disease diagnosis device that includes a measurement means configured to measure one index or more selected from the group consisting of superoxide production activity, myeloperoxidase activity, oxidized LDL level, phagocytosis, triglycerides, fasting blood glucose, total cholesterol, hemoglobin A1c, and insulin in peripheral blood and a displaying means configured to display an index measured by the measurement means as a pathological index for Alzheimer's disease.

Abstract: The present invention relates to a method of evaluating neutrophil activity, which includes: evaluating neutrophil activity based on an index derived from measurement results of myeloperoxidase (MPO) activity or superoxide production of a biological sample to which a neutrophil stimulant is added, in which the index is a time from addition of the neutrophil stimulant to rise of a peak of the MPO activity or the superoxide production.

Abstract: Provided is a measurement container including a container body where a first region, a second region, and an intermediate region are continuously formed as an accommodation space accommodating a sample and an inlet is formed and a rotor which is arranged in the second region and rotated by an effect of magnetic force. The container body includes a wall portion which defines the accommodation space and at least a portion of which has a light transmitting property and a partitioning portion which partitions the intermediate region into one side and the other side in a second direction perpendicular to the first direction. The partitioning portion partitions the intermediate region into the one side and the other side so that a communication region which allows the one side and the other side to communicate with each other in the intermediate region remains.

Abstract: The present invention provides a method for preparing algal cells used for evaluating a toxicity of a chemical substance by delayed luminescence, the method comprising the step of freezing algal cells in a logarithmic growth phase.

Abstract: A measurement apparatus includes a sample stage, an excitation unit, a light receiving unit, a stimulant applying nozzle, and a spray nozzle in a measurement space inside a body case, and also includes a heating unit and a gas supplying unit. The body case includes an inner case surrounding the measurement space, and an outer case surrounding the inner case to shield the measurement space from light from the outside and seal the measurement space. The heating unit is disposed between the inner case and the outer case and adjusts temperature in the measurement space through the inner case. The gas supplying unit supplies gas having controlled temperature and humidity into the measurement space and adjusts temperature and humidity in the measurement space.

Abstract: The present invention relates to a method for evaluating phagocytic capacity of phagocytes, including incorporating a fluorescent substance into phagocytes in a sample containing whole blood to obtain a measurement sample, standing the measurement sample for 2 minutes or more, measuring the fluorescence of the fluorescent substance, and evaluating the phagocytic capacity of phagocytes based on the intensity of the measured fluorescence, in which the measuring the fluorescence of the fluorescent substance includes irradiating an intermediate region of gravity direction of a placed measurement sample with an excitation light, and detecting the fluorescence generated from the fluorescent substance by the excitation light.

Abstract: A measurement apparatus includes a sample stage, an excitation unit, a light receiving unit, a stimulant applying nozzle, and a spray nozzle in a measurement space inside a body case, and also includes a heating unit and a gas supplying unit. The body case includes an inner case surrounding the measurement space, and an outer case surrounding the inner case to shield the measurement space from light from the outside and seal the measurement space. The heating unit is disposed between the inner case and the outer case and adjusts temperature in the measurement space through the inner case. The gas supplying unit supplies gas having controlled temperature and humidity into the measurement space and adjusts temperature and humidity in the measurement space.

Abstract: An object of the present invention is to appropriately and easily evaluate a photosynthetic function of a photosynthetic sample contained in an evaluation sample. An evaluation method for photosynthetic sample according to the present invention is for evaluating a state of a photosynthetic sample with a photosynthetic function based on temporal data of a luminescence amount of delayed luminescence emitted from the photosynthetic sample. First, characteristic values that indicate characteristics are determined for a plurality of time periods in the temporal data. An evaluation value is then computed by weighting the characteristic values. The state of the photosynthetic sample is then evaluated based on the evaluation value.

Abstract: The present invention provides a method for evaluating the toxicity of a chemical by using an alga, comprising: (a) a thawing step of thawing frozen algal cells by heating, and diluting the obtained suspension of the cells by adding a culture medium thereto; (b) a recovery culture step of culturing the algal cells obtained in the thawing step (a) to allow the algal cells to recover from the effects of freezing and thawing; (c) a confirmation step of collecting a part of the algal cells after the recovery culture step (b), diluting the part of the algal cells by adding a culture medium thereto, and measuring the amount of the luminescence of the delayed luminescence of the algal cells as initial value data; (d) an exposure step of mixing the algal cells after the confirmation step (c) with a solution containing a test substance to prepare an exposure sample, and culturing the exposure sample; (e) a measurement step of measuring the amount of the luminescence of the delayed luminescence of the exposure sample a

Abstract: The present invention provides a method for preparing algal cells used for evaluating a toxicity of a chemical substance by delayed luminescence, the method comprising the step of freezing algal cells in a logarithmic growth phase.

Abstract: The present invention provides a method for evaluating the toxicity of a chemical by using an alga, comprising: (a) a thawing step of thawing frozen algal cells by heating, and diluting the obtained suspension of the cells by adding a culture medium thereto; (b) a recovery culture step of culturing the algal cells obtained in the thawing step (a) to allow the algal cells to recover from the effects of freezing and thawing; (c) a confirmation step of collecting a part of the algal cells after the recovery culture step (b), diluting the part of the algal cells by adding a culture medium thereto, and measuring the amount of the luminescence of the delayed luminescence of the algal cells as initial value data; (d) an exposure step of mixing the algal cells after the confirmation step (c) with a solution containing a test substance to prepare an exposure sample, and culturing the exposure sample; (e) a measurement step of measuring the amount of the luminescence of the delayed luminescence of the exposure sample a

Abstract: An object of the present invention is to appropriately and easily evaluate a photosynthetic function of a photosynthetic sample contained in an evaluation sample. An evaluation method for photosynthetic sample according to the present invention is for evaluating a state of a photosynthetic sample with a photosynthetic function based on temporal data of a luminescence amount of delayed luminescence emitted from the photosynthetic sample. First, characteristic values that indicate characteristics are determined for a plurality of time periods in the temporal data. An evaluation value is then computed by weighting the characteristic values. The state of the photosynthetic sample is then evaluated based on the evaluation value.