Sony Corporation

Kyoto University

Suguru Dowaki

Eriko Matsui

Hirokazu Tatsuta

Shiori Oshima

Shin Hasegawa

Shingo Imanishi

Gakuji Hashimoto

Takeshi Kunihiro

Eiichi Tanaka

Tomohiro Hayakawa

Tatsutoshi Nakahata

Megumu Saito

Akira Niwa

Shunpei Suzuki

Tatsuya Minakawa

Kazuhiro Nakagawa

Shinsuke Haga

Masanobu Tamai

Hiroaki Morikawa

Disclosed is a technology for illuminating a specimen in a desired uniform illumination pattern and capturing an image of a wide field of view in a low background illumination environment. Provided, for example, is a fluorescence microscope apparatus including a first illumination optics, a second illumination optics, and an imaging optics. The first illumination optics includes a first light source for exciting fluorescence in a specimen, a spatial light modulation element, and a first illumination optical member for uniformly illuminating the spatial light modulation element. The second illumination optics includes a second illumination optical member for forming an image of a light beam from the spatial light modulation element on a specimen surface. The imaging optics includes an imaging optical member and an imaging element. The imaging optical member captures an image of the specimen surface.

Fluorescence microscope apparatus and fluorescence microscope system

An optical microscope device includes: a first illumination optical system including a light source that emits illumination light for illuminating a specimen an LCOS spatial light modulation element that controls a polarization state of the illumination light, a first illumination optical member that uniformly illuminates the LCOS spatial light modulation element, and a polarization optical element that controls a transmission state of the illumination light directed to the specimen from the LCOS spatial light modulation element in response to the polarization state of the illumination light; a second illumination optical system including a second illumination optical member that images a light flux from the first illumination optical system on a specimen surface; and an imaging optical system for imaging the specimen surface.

Optical microscope and system including illumination to change function of biomaterial

An observation system includes a microscope optical system, an image pickup unit, an image pickup control unit, a detection unit, and an observation control unit. The image pickup unit is configured to take an image of a field-of-view range of the microscope optical system. The image pickup control unit is configured to cause the image pickup unit to take images of an observation sample in the field-of-view range at a plurality of focal positions and generate detection images. The detection unit is configured to detect a three-dimensional position of an observation target object in the observation sample from the detection images. The observation control unit is configured to fit the field-of-view range of the microscope optical system to the three-dimensional position.

Observation system, observation program, and observation method

There is provided an image processing apparatus including a motion detector that detects motion of an observation target from a hologram of the observation target, a hologram processing unit that extracts a portion of the hologram based on a result obtained by detecting the motion of the observation target, and a reconstruction unit that reconstructs an image from a portion of the extracted hologram.

Image processing apparatus, method of image processing, and image processing system

A culture container includes a first transparent member being capable of keeping a predetermined temperature; a second transparent member facing to the first transparent member; a housing member to which the first transparent member and the second transparent member are adhered forming a culture space being capable of housing a well plate together with the first transparent member and the second transparent member; and a sealing member for sealing a liquid injected into the culture space between the first transparent member and the housing member.

Culture container, culture observation apparatus and culture observation method

To provide an image processing apparatus, an image processing program, an image processing method, and a microscopic system that are capable of acquiring a high-resolution image that is suitable for scientific verification. An image processing apparatus according to the present technology includes an image conversion unit and an image generation unit. The image conversion unit converts a first picked-up image and a second picked-up image into frequency components, the first picked-up image being obtained by picking up an image of an observation target object with first illumination light via a microscope optical system, the second picked-up image being obtained by picking up an image of the observation target object with second illumination light via the microscope optical system, the second picked-up image having a contrast in a low frequency band lower than that of the first picked-up image and a contrast in a high frequency band higher than that of the first picked-up image. The image generation unit combines a low frequency component of the first picked-up image and a high frequency component of the second picked-up image with each other to generate a composite image.

Image processing apparatus, image processing program, image processing method, microscopic system

As a result of acquiring visible absorption spectra of red blood cells and analyses of the spectra, inventors of the present disclosure have discovered the fact that echinocytes show a characteristic spectrum pattern having an absorption peak in a wavelength region of 450 to 490 nm between Soret and Q bands. Then, the present disclosure provides a blood analysis apparatus having an analysis section for detecting the absorption peak of a visible absorption spectrum acquired for blood. In accordance with this blood analysis apparatus, on the basis of the absorption peak, it is possible to detect echinocytes contained in blood.

Detecting echinocytes in blood

An observation apparatus according to the present technology includes a microscope optical system, an imaging unit, a spectroscopic unit, and a detection unit. The imaging unit captures an image via the microscope optical system. The spectroscopic unit acquires an absorption spectrum or a Raman spectrum in an ultraviolet, visible, or infrared area via the microscope optical system. The detection unit detect an observation target object in an observed sample by using the absorption spectrum or the Raman spectrum.

Image analysis using microscope optical system

[Object] To provide an image processing apparatus, an image processing program, and an image processing method capable of obtaining three-dimensional information of an observation target object. [Solving Means] An image processing apparatus includes a difference calculation unit and a difference distribution generation unit. The difference calculation unit calculates, for each of pixels that constitute a pickup image in each of a plurality of pickup images taken at different focal depths, a difference of a luminance value from an adjacent pixel. A difference image generation unit generates, on the basis of the difference and the focal depth at which the pickup image including the pixel whose difference is calculated is taken, a distribution of the difference with respect to the focal depth.

Image processing apparatus, image processing program, and image processing method

Disclosed herein is an optical measuring device including: a light applying section configured to apply exciting light to a sample flowing in a channel; and a scattered light detecting section configured to detect scattered light generated from the sample irradiated with the exciting light on the downstream side of the sample in the traveling direction of the exciting light; the scattered light detecting section including a scattered light separating mask for separating the scattered light into a low numerical aperture component having a numerical aperture not greater than a specific value and a high numerical aperture component having a numerical aperture greater than the specific value; a first detector for detecting the low numerical aperture component; and a second detector for detecting the high numerical aperture component.

Optical measuring device and optical measuring method

An analysis apparatus includes a two-dimensional coordinate detecting unit and a three-dimensional coordinate determining unit. The two-dimensional coordinate detecting unit is configured to detect, with respect to a captured image group obtained by capturing an analysis specimen including an analysis target object at a plurality of focal depths, a two-dimensional coordinate candidate being a candidate of a plane coordinate of the analysis target object in each captured image. The three-dimensional coordinate determining unit is configured to determine, based on a position relationship of the plane coordinate candidates between the captured images, a three-dimensional coordinate candidate being a candidate of a three-dimensional coordinate of the analysis target object.

Analysis apparatus, analysis program, and analysis system

There is provided a measurement apparatus including an objective lens, a stage, a setting unit, and a controller. The stage is configured to support a sample vessel in which a plurality of wells each containing a sample are arranged and to define relative positions of the sample vessel and the objective lens. The setting unit is configured to determine whether to set each of the plurality of wells to be a measurement target and set the measurement target. The controller is configured to control the stage such that a well determined to be the measurement target by the setting unit and the objective lens face each other.

Measurement apparatus, program, and measurement method

Disclosed is a fine particle measurement apparatus including a light condensing unit that condenses irradiated light irradiated to a sample flow where fine particles pass through and directly propagates the light without scattering, and scattered light scattered by the fine particles to an optical receiver divided into a plurality of regions; a position controller that controls the relative positions of members of an optical path; and a control unit that detects positions of condensing spots of the irradiated light and the scattered light based on signal intensities of each region of the optical receiver, and controls the position controller such that the positions of the condensing spots of the irradiated light and the scattered light match with each other.

Growing community of inventors

Kanagawa, Japan

Suguru Dowaki