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∙ 11y agomagnification= ocular power *objective power=10X*60X
Wiki User
∙ 13y agoThe total magnification would be 10x (ocular lens) multiplied by 25x (objective lens), which equals 250x magnification.
Wiki User
∙ 11y ago250x
Wiki User
∙ 10y ago50x
To determine the total magnification when using any objective of your microscope, you need to multiply the magnification of the objective lens by the magnification of the eyepiece. The total magnification is equal to the product of these two magnifications.
The magnification of a telescope is calculated by dividing the focal length of the telescope by the focal length of the eyepiece. In this case, the magnification would be 3000 mm (telescope focal length) divided by 15 mm (eyepiece focal length), which equals a magnification of 200x.
When using a 100X objective lens, you typically want to use a high numerical aperture (NA) condenser lens to match the high NA of the objective lens. A condenser with a NA value equal to or greater than the NA of the objective lens (typically around 1.4) is recommended for optimal resolution and contrast in microscopy.
The limit of resolution of a light microscope is determined by the wavelength of light used and the numerical aperture of the lenses. Smaller wavelengths and higher numerical apertures result in better resolution. However, there is a physical limit to the resolution of light microscopes due to diffraction.
The main lens or mirror produces a virtual image of the obect being looked at, and it occurs at a distance behind the lens (or in front of the mirror) equal to the focal length. The telescope also has an eyepiece whose function is to allow the oberver to see the virtual image. Many telescopes come with a range of different eyepieces that give different amounts of magnification.
The total magnification is equal to the magnification of the eyepiece multiplied by the magnification of the objective lens. So in this case the objective lens would need to be 100X.
The magnification in a microscope is the same for both length and width measurements when using the same objective lens. The magnification factor is determined by the combination of the objective and ocular lenses in the microscope, resulting in equal magnification for both dimensions.
To determine the total magnification when using any objective of your microscope, you need to multiply the magnification of the objective lens by the magnification of the eyepiece. The total magnification is equal to the product of these two magnifications.
1 ocular micrometer scale is equal to 1micrometer when it is seen from 10X objective it will be magnify by 100 times so, 1 ocular micrometer division become 0.1mm ( 1um * 100 = 0.1mm)
If the focal lengths of the objective and eyepiece are equal,then the magnification is ' 1 '.
The objective lens (right above the slide stage) is 4x. The eyepiece (what you look into) is 10x. 4 times 10 = 40. Whatever the objective lens power is, you have to multiply it by the eyepiece power (usually 10x) to get the overall magnification.
Parfocal capability refers to the ability of a lens system, such as a microscope or a camera lens, to remain in focus when magnification is changed. This means that once the focus is set at a particular magnification, the image will stay relatively sharp when switching to a different magnification level without the need for major adjustments.
Yes, the magnification of an optical system is equal to the size of the image divided by the size of the object. Magnification describes how much larger an object appears through the optical system compared to its actual size.
Objective
To make all the powers more equal
The magnification of a telescope is calculated by dividing the focal length of the telescope by the focal length of the eyepiece. In this case, the magnification would be 3000 mm (telescope focal length) divided by 15 mm (eyepiece focal length), which equals a magnification of 200x.
To find the diameter of the cell, you need to first calculate the calibration factor by dividing the number of stage micrometer divisions by the number of ocular divisions that line up. In this case, the calibration factor would be 2/13. Then, use the calibration factor to determine the size of the cell that spans 16 ocular divisions. In this scenario, the diameter of the cell would be 16 * calibration factor.