Abstract: An in-vivo examination apparatus in which the examination angle can be changed while keeping an examination site in focus to carry out accurate in-vivo examination is provided. The in-vivo examination apparatus includes a stage on which a living organism is mounted, a measurement head that irradiates the living organism on the stage with light emitted from a light source and detects light returning from the living organism, and a rotation mechanism that rotates the measurement head about a fixed point on the stage.

Abstract: A fluorescent microscope comprises a light source, an optical illumination system which forms an optical path to irradiate a specimen with a light beam from the light source, an objective lens which condenses the light beam of the optical illumination system onto the specimen, an optical device which is disposed on the optical path of the optical illumination system and which decenters the light beam by decentering an optical axis of the optical path, and a slit which passes the light beam decentered by the optical device through a total reflection illumination region on an emission pupil surface of the objective lens.

Abstract: A fluorescent microscope comprises a light source, an optical illumination system which forms an optical path to irradiate a specimen with a light beam from the light source, an objective lens which condenses the light beam of the optical illumination system onto the specimen, an optical device which is disposed on the optical path of the optical illumination system and which decenters the light beam by decentering an optical axis of the optical path, and a slit which passes the light beam decentered by the optical device through a total reflection illumination region on an emission pupil surface of the objective lens.

Abstract: A recording apparatus includes a recording unit for effecting recording on a recording medium, and a conveying unit for conveying the recording medium. The recording apparatus further includes a power input terminal adapted to be switched ON/OFF by the ignition key switch of an automobile, and a controller for executing the operation sequence of the recording apparatus in accordance with the ON/OFF state of the power input terminal. In addition, a method of controlling the above-described recording apparatus includes executing the operation sequence of the recording apparatus in accordance with the ON/OFF state of the power input terminal switched ON/OFF by the ignition key switch of an automobile.

Abstract: A microscope includes an illuminating unit that includes an excitation light source emitting an excitation light, and a phosphor receiving the excitation light and emitting illumination light in a specific wavelength range. The illuminating unit illuminates a specimen with the illumination light. The microscope also includes an observation unit for observing the specimen illuminated by the illuminating unit.

Abstract: An observation apparatus includes an incident-light illumination optical system, a transmitting illumination optical system, an imaging unit, an input device, a storage unit, an imaging controller, a microscope controller, an imaging information management unit. The imaging information management unit compares an area position, of an imaging area of the imaging unit, indicated by position information input from the input device with an area position stored in the storage unit to determine whether the area position indicated by the position information is stored in the storage unit. When the area position is not stored in the storage unit, the imaging controller controls the imaging unit to image the specimen and to generate an observation image, and stores the observation image in the storage unit. The microscope controller controls one of the optical systems to illuminate the specimen only during an imaging period, when the imaging unit images the specimen.

Abstract: An observation apparatus includes an illuminating unit that illuminates a sample; an imaging unit that captures an image of the sample to generate an observation image; a storage unit that stores the observation image in association with an illumination condition of the illuminating unit at generation of the observation image by the imaging unit; an imaging controller that controls the imaging unit to capture the image of the sample to generate the observation image and stores the observation image in the storage unit; and an illumination controller that controls the illuminating unit to illuminate the sample, and stores the illumination condition in the storage unit every time the imaging unit captures the image of the sample.

Abstract: A tissue culture microscope apparatus includes a culture unit that includes a chamber in which a specimen is put, and maintains the chamber at a predetermined temperature to culture the specimen; an observation unit that forms an observation image of the specimen put in the chamber; and a liquid supply unit that stores a liquid in a protrusion portion penetrating into a wall of the chamber and protruding to an inside of the chamber, matches a temperature of the liquid with the temperature of the chamber, and injects the liquid from the protrusion portion to the specimen.

Abstract: An observation apparatus includes an illumination unit that illuminates a specimen; an imaging unit that captures an image of the specimen to generate an observation image; and an imaging and display controller that controls the imaging unit so that an image of the specimen is preliminary captured to generate a preliminary observation image, and controls a display unit so that the preliminary observation image is displayed. The apparatus also includes a storage controller that stores, in a storage unit, a position selected based on the preliminary observation image and employed as a main observation position for a main observation of a partial region inside the specimen; and an illumination controller that controls the illumination unit so that the specimen is illuminated only in a time period during which the imaging unit captures an image of the specimen, at least when the imaging unit generates the preliminary observation image.

Abstract: Provided is a microscope having an immersion objective lens, a nozzle, and a liquid supplying mechanism. The immersion objective lens condenses light from a sample through liquid. The nozzle supplies the liquid to an upper surface of the immersion objective lens. The liquid supplying mechanism cooperates with one of a lens moving mechanism that moves the immersion objective lens and a sample moving mechanism that maintains and moves the sample, and moves the nozzle relative to the immersion objective lens to supply the liquid.

Abstract: A focus detection device which is applied to a fluorescent observation device for observing a fluorescent image to be emitted from an observation sample on the basis of an evanescent light, includes an image pickup unit which detects a contrast of the fluorescent image by imaging the fluorescent image, and a detector which detects a focus on the basis of the detection result.

Abstract: A culture observation apparatus, which is used for observing a cultured cell while culturing the cell, includes a culture device that forms a culture space which is controlled to be an environment suitable for culturing the cultured cell; a sample tray that holds a container housing the cultured cell and a culture medium; a microscope that serves for observing the cultured cell; a tray holding mechanism that holds the sample tray in the culture space in a detachable manner with good reproducibility; and a shifting mechanism that relatively shifts the sample tray held by the tray holding mechanism and a light axis of the microscope along a plane that is orthogonal to the light axis, wherein the sample tray has a heater used for heating the sample tray, and is electrically connectable to an energy supplying unit that supplies energy to the sample tray.

Abstract: A culture observation apparatus, which is used for observing a cultured cell while culturing the cell, includes a culture device that cultures the cultured cell, and a microscope used for observing the cultured cell. The culture device includes a first space that is controlled to an environment suitable for culture of the cell, and a second space that is controlled to a lower humidity condition in comparison with the first space. The microscope includes an objective optical unit including an objective lens; the objective optical unit having at least one portion located in the second space, and another portion extending into the first space through an opening formed in a partition wall that separates the first space and the second space, with a gap between the objective optical unit and the partition wall being sealed by a sealing member, and the objective lens includes a plurality of lens groups, with mutual spaces among the lens groups vented to the second space.

Abstract: An observation apparatus includes a sample tray that holds a container housing a cultured cell and a culture medium and covered with a lid; an observation unit that serves for observation of the cultured cell; and a shifting unit that relatively shifts the sample tray and a light axis of the observation unit along a plane that is orthogonal to the light axis of the observation unit, wherein the sample tray includes a container holding unit that holds the container by utilizing an elastic force, and at least one of the lid and one portion of the lid is made detachable, with the container being held in the sample tray by the container holding unit.

Abstract: A microscope includes a high humidity space that is maintained at a predetermined gas temperature and a predetermined relative humidity for culture of a living sample; an objective lens having a tip portion with a top lens which is disposed in the high humidity space, and serving to allow for an observation of the living cell incubated inside the high humidity space; a heater that heats the objective lens; and a temperature controller that controls the heater so that a surface temperature and an internal temperature of the objective lens are higher than a dew-point temperature and lower than a thermal death point of the living sample.

Abstract: The invention reduces the loss of fluorescence intensity obtained from a specimen to acquire clear fluorescence images when irradiating the specimen with ultrashort-pulse laser light produced by a laser light source. The invention provides a laser-scanning examination apparatus including a laser light source for producing ultrashort-pulse laser light; a laser light source for producing continuous-wave laser light; a measurement head including an optical scanning unit for scanning the laser light on a specimen and an objective optical system; an imaging unit for detecting return light from the specimen in response to the ultrashort-pulse laser light; and an imaging unit for detecting return light from the specimen in response to the continuous-wave laser light. The laser light sources and one imaging unit are connected to the measurement head by an optical fiber, and the other imaging unit is connected to the measurement head by another optical fiber with a larger core diameter.

Abstract: An in-vivo examination apparatus in which the examination angle can be changed while keeping an examination site in focus to carry out accurate in-vivo examination is provided. The in-vivo examination apparatus includes a stage on which a living organism is mounted, a measurement head that irradiates the living organism on the stage with light emitted from a light source and detects light returning from the living organism, and a rotation mechanism that rotates the measurement head about a fixed point on the stage.

Abstract: A microscope has an objective lens for observation of a specimen, light-emitting diodes with different emission wavelengths, a wavelength multiplexing device that multiplexes light emitted from the light-emitting diodes, and an illumination optical system that forms the multiplexed light into an image on a rear focal plane of the objective lens. All the light-emitting diodes being in a positional relationship conjugate to a rear focus of the objective lens through the wavelength multiplexing device and the illumination optical system. The microscope also has a photometric device that measures light from the specimen, an image sensing device that senses an image of the specimen through the objective lens, and a power supply device that controls brightness of light emitted from the light-emitting diode on the basis of a photometric value obtained by the photometric device.

Abstract: A focusing method for an examination apparatus that can quickly and easily perform focusing for fluoroscopy is provided. The focusing method, for an examination apparatus that can observe fluorescence emitted from a specimen, includes a first step of irradiating the specimen with light via an objective lens to generate reflected light and fluorescence; a second step of performing focusing with respect to the surface of the specimen using the reflected light from the specimen; and a third step of performing focusing for the fluorescence based on the focal position of the specimen surface in the second step.

Abstract: A system microscope includes a microscope body, a stage which is provided on an upper portion of the microscope body and on which a sample is placed, a lower objective lens provided below the stage, an upper objective lens provided above the stage, a portal support member which is provided on the upper portion of the microscope body so as to straddle the stage, a lower illumination device which is provided for the microscope body and illuminates the sample from below, an upper illumination device which is provided on the portal support member and illuminates the sample from above, a lower eyepiece lens which is provided for the microscope body and acquires an observation image of the sample from the lower objective lens, and an upper eyepiece lens which is provided on the portal support member and acquires an observation image of the sample from the upper objective lens.