Abstract:
Provided is a laser scanning microscope including a stage on which a sample is placed, an objective lens that is disposed below the stage and that focuses laser light from a light source onto the sample, a scanner that scans the laser light focused by the objective lens over the sample, a condenser lens disposed opposite the objective lens with the stage interposed therebetween, and a light blocking cover that is disposed in an optical path between the condenser lens and the stage and that blocks external light entering the objective lens or the condenser lens from above the sample via the stage.
Abstract:
The number of detection channels of detecting sections is increased and the detecting sections are replaced easily and at low cost while suppressing loss in the quantity of returning light. Provided is a detection unit (5A) including a detector entrance port (75A) through which light in a predetermined optical form enters, a detector (57A) that detects at least a portion of the light entering through the detector entrance port (75A), and a detector exit port (65A) through which at least another portion of the light entering through the detector entrance port (75A) can exit in the same optical form.
Abstract:
An inverted microscope system includes an objective lens holding unit that holds an objective lens configured to collect at least observation light from a specimen, a tube lens configured to form an image using the observation light collected by the objective lens, a total internal reflection fluorescence microscopy optical system provided between the objective lens and the tube lens and configured to observe the observation light from the specimen using a total reflection illumination, and a disk scanning confocal optical system including a rotary disk on which a confocal opening is formed, the confocal opening being placed at a position substantially conjugate to a focus position of the objective lens. A relative distance between the focus position of the objective lens and the substantially conjugate position is changeable along an optical path of the observation light.
Abstract:
An inverted microscope includes an imaging lens configured to form an image of light which passes through an objective lens from a specimen, and a microscope main body in which a plurality of optical devices are configured to be arranged between the objective lens and the imaging lens in a direction of an optical axis of the objective lens and which includes therein a plurality of installation units that allow the plurality of optical devices to be fixed independently of one another. Each of the plurality of installation units includes an abutting reference surface on which any one of the plurality of optical devices is configured to be abutted. A plurality of abutting reference surfaces of the plurality of the installation units are shifted from one another in a direction perpendicular to the optical axis of the objective lens.
Abstract:
A microscope focusing mechanism includes a fixing part attached to a microscope main body, a fixing-side guide member attached to the fixing part, a plate-shaped base part that supports at least one of a stage for placing a specimen and a revolver to which multiple objective lenses are detachably attached, a moving-side guide member that is fixed to the base part, that is connected to the fixing-side guide member, and that is movable in a direction of an optical axis of one of the objective lenses, and a plate member that is arranged on a side of the base part opposite to a side where the moving-side guide member is arranged. A linear expansion coefficient of a material of each of the moving-side guide member and the plate member differs from a linear expansion coefficient of a material of the base part.