Abstract: An object of the present invention is to provide a predetermined site luminescence measuring method and a predetermined site luminescence measuring apparatus, which allow for determining whether, when the luminescence from the predetermined site in live samples is measured, a photoprotein is localized at the predetermined site in the same ones as the samples.

Abstract: An object of the present invention is to provide a predetermined site luminescence measuring method and a predetermined site luminescence measuring apparatus, which allow for determining whether, when the luminescence from the predetermined site in live samples is measured, a photoprotein is localized at the predetermined site in the same ones as the samples.

Abstract: The present invention is related to a method of analyzing an optical signal which analyzes a signal substance induced by a photosensitive protein, includes the steps of introducing a gene which expresses a luminescent probe to analyze the signal substance into an organism sample, emitting a stimulus light to activate the photosensitive protein, and detecting an optical signal emitted by the organism sample.

Abstract: There is provided a novel luminescence measuring apparatus that enables measuring a luminescence amount or a luminescence intensity from plural living biological samples, such as tissues, cells, and biological individuals, into which a gene expressing a luminescent protein has been introduced, individually for the respective biological samples. The inventive luminescence measuring apparatus comprises an image acquisition portion that acquires a luminescence image of biological samples; a measurement region determination portion that determines at least one measurement region in the luminescence image; and a luminescence measurement portion that measures the luminescence amount or luminescence intensity in the determined measurement region; thereby measuring the luminescence amount or luminescence intensity individually by the biological sample(s) included in the measurement region. Irrespective of an efficiency of transfer of a luminescent protein gene into a cell, etc.

Abstract: A novel apparatus and a novel method of imaging a luminescence phenomenon of a sample of biological origin using an optical image formation device are provided. In the inventive method and apparatus, an illumination image acquired by illuminating the sample and a luminescence image acquired with the light emitted by a luminescence phenomenon of a cell in the sample without illuminating it are superposed to generate a superposition image. In the superposition image, an analysis region is determined. Thereby, even when the light detected in a luminescence observation is feeble, a luminescent cell and/or a luminescent site in a cell in a sample can be specified.

Abstract: Disclosed is a luminescence measuring method which can produce a luminous intensity depending on the amount of a substance to be measured even when the substance occurs in a biological sample in an amount equal to or more than a given amount, and which can achieve quantitative measurement. The method is characterized by includes preparing a biological sample containing a luminescence-associated protein which is can react with a substance occurring in the biological sample in amount equal to or more than a given amount and which has a Km value equal to or higher than a predetermined value so that the luminous intensity can be quantified depending on the amount of the substance, measuring the luminescence intensity emitted from the biological sample, and outputting a result of the measurement on a regions and/or part of the biological sample.

Abstract: A paste for a secondary battery electrode, comprising an electrode active material and a polymer composition comprising (a) a fluorine-containing polymer and (b) a functional group-containing polymer which contains a structural unit originating from an alkyl (meth)acrylate and a structural unit originating from at least one monomer selected from the group consisting of a sulfonic acid group-containing unsaturated monomer, an amide group-containing unsaturated monomer, and a sulfonic acid group and amide group-containing unsaturated monomer is provided.

Abstract: In order to be able to take an image of a specimen emitting low light in a short exposure time by a cooled CCD at about 0° C., a low-light specimen image pickup unit has an imaging optical system forming a specimen image of a specimen having a point light source emitting a low light, and the low-light specimen image pickup unit further has an image pickup unit having a plurality of pixels receiving incident light, for taking an image corresponding to the specimen image. In the low-light specimen image pickup unit, the imaging optical system is telecentric to a side of the specimen image of the imaging optical system, and condenses the low light emitted from the point light source to form an Airy disk of a size which is substantially the same as a pixel of the pixels, or which is smaller than the pixel. Here, the pixel receives the low light emitted from the point light source.

Abstract: There is provided a binder composition for secondary battery electrode, containing (A) a sulfonic acid group-containing polymer, and (B) an organic solvent composed mainly of N-methylpyrrolidone, wherein the proportion of the sulfonic acid group in the polymer (A) is 0.005 to 1.0 mmol/g.

Abstract: An object of the present invention is to provide a predetermined site luminescence measuring method and a predetermined site luminescence measuring apparatus, which allow for determining whether, when the luminescence from the predetermined site in live samples is measured, a photoprotein is localized at the predetermined site in the same ones as the samples.

Abstract: A polymer composition comprising (a) a fluorine-containing polymer and (b) a functional group-containing polymer which contains a structural unit originating from an alkyl (meth)acrylate and a structural unit originating from at least one monomer selected from the group consisting of a sulfonic acid group-containing unsaturated monomer, an amide group-containing unsaturated monomer, and a sulfonic acid group and amide group-containing unsaturated monomer is provided.

Abstract: An imaging section inputs rays of light from a subject through a lens and forms an image of the subject. A display screen of a display section displays an image of a subject focused by the lens. A focus area selecting section selects one of a plurality of focus areas displayed on the display screen. A focus adjusting section adjusts a focus on the subject in the selected focus area. A crop section automatically selects a crop area corresponding to the selected focus area and captures as a crop image an image in the selected crop area. The photographer can easily obtain a crop image by photographing a subject according to a conventional procedure.

Abstract: In a biological specimen imaging method, a biological specimen which is stored in a storing section of a substrate having plural storing sections and emitting a feeble light is imaged through an objective lens. The biological specimen imaging method includes moving any one of the substrate and the objective lens or both until the desired storing section falls within the field of view of the objective lens, measuring any one of a focal position at a near point and the focal position at a far point of the objective lens or both, determining the focal position of the objective lens focused on an observed target region in the biological specimen stored in the desired storing section based on the measured focal position, and adjusting the focal position of the objective lens to the determined focal position so as to image the biological specimen through the objective lens.

Abstract: A focal position determining method determines a focal position of an objective lens focused on an observed target region in a specimen. The focal position determining method includes measuring any one of the focal position of the objective lens at a near point and the focal position of the objective lens at a far point or both so as to determine the focal position of the objective lens focused on the observed target region based on the measured focal position.

Abstract: In order to be able to take an image of a specimen emitting low light in a short exposure time by a cooled CCD at about 0° C., a low-light specimen image pickup unit has an imaging optical system forming a specimen image of a specimen having a point light source emitting a low light, and the low-light specimen image pickup unit further has an image pickup unit having a plurality of pixels receiving incident light, for taking an image corresponding to the specimen image. In the low-light specimen image pickup unit, the imaging optical system is telecentric to a side of the specimen image of the imaging optical system, and condenses the low light emitted from the point light source to form an Airy disk of a size which is substantially the same as a pixel of the pixels, or which is smaller than the pixel. Here, the pixel receives the low light emitted from the point light source.

Abstract: In an authentication matching method and device which provide an optimum service to a user in view of a network condition in a state where the user is authenticated, access from the user is authenticated, an optimum network condition and service are selected, when the access is authenticated, from a database depending on a condition which the user desires to use, and the user is connected to a network connection device and a service providing device respectively corresponding to the network condition and service selected.

Abstract: It is an object to provide a luminescent sample imaging method, a luminescent cell imaging method and an objective lens capable of capturing a clear image in short exposure time, or even in real time. The luminescent sample imaging method of the present invention captures a clear image in short exposure time, or even in real time from the luminescent sample 1 using an objective lens 2 having a value of (NA÷?)2 represented by numerical aperture (NA) and projection magnification (?) of equal to or more than 0.01, a condenser lens 3, a CCD camera 4 and a monitor 5.

Abstract: A reliability authorizing device determines whether to authorize a service transfer based on reliability of a partner device or a partner user when one user of one device authenticates other user of other device to exchange the service between devices connected to a network. A partner-reliability collecting unit collects reliability of the partner device or the partner user. A partner-reliability providing unit provides the reliability of the partner device or the partner user collected by the partner-reliability collecting unit.

Abstract: A security server monitoring device is provided that performs quick redistribution of loads when a server load increases due to virus infections. A security server performs a virus check on data flowing through a network, thus statistical data relating to detected viruses can be obtained. For example, future communication traffic and increases and decreases in server loads are predicted using statistical information such as the number of virus infections (number of virus infections per unit of time), and on the basis of this prediction, a security server allocated to a path is quickly changed from a security server in which a high load is predicted to a security server with a comparably low load.

Abstract: The present invention provides a method of detecting a micronucleus in a living cell to be measured, without having to fixate the cell, characterized by comprising generating a mother cell by introducing a gene encoding a single or a plurality of nucleus-related proteins and a gene encoding a fluorescence protein into a culture cell, and making then expressed in the cell, subjecting the cell to a treatment for a toxicity test or a mutagenicity test of a test substance, performing a limited excitation which makes a region of the micronucleus emit fluorescence limitedly, and quantitatively measuring an amount of the fluorescence corresponding to a component of the nucleus-related protein.