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Parfocal microscope objectives stay in focus when magnification is changed; i.e., if the microscope is switched from a lower power objective (e.g., 10×) to a higher power objective (e.g., 40×), the object stays in focus. Most modern bright-field microscopes are parfocal.
The oil is applied to the specimen (conventional microscope), and the stage is raised, immersing the objective in oil. (In inverted microscopes the oil is applied to the objective). The refractive indices of the oil and of the glass in the first lens element are nearly the same, which means that the refraction of light will be small upon ...
Two Leica oil immersion microscope objective lenses; left 100×, right 40×. The objective lens of a microscope is the one at the bottom near the sample. At its simplest, it is a very high-powered magnifying glass, with very short focal length. This is brought very close to the specimen being examined so that the light from the specimen comes ...
A compound microscope uses a lens close to the object being viewed to collect light (called the objective lens), which focuses a real image of the object inside the microscope. That image is then magnified by a second lens or group of lenses (called the eyepiece ) that gives the viewer an enlarged inverted virtual image of the object.
In both cases the numerical aperture of the objective is 1.49 and the refractive index of the medium 1.52. The wavelength of the emitted light is assumed to be 600 nm and, in case of the confocal microscope, that of the excitation light 500 nm with circular polarization. A section is cut to visualize the internal intensity distribution.
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Memorial in Jena, Germany to Ernst Karl Abbe, who approximated the diffraction limit of a microscope as = , where d is the resolvable feature size, λ is the wavelength of light, n is the index of refraction of the medium being imaged in, and θ (depicted as α in the inscription) is the half-angle subtended by the optical objective lens (representing the numerical aperture).
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