Magnification and resolution

Cell Structure, Reproduction and Development · Microscopy and measuring cells · note 1 of 3

Magnification and resolutionSpec 3.7

In short

Magnification is how many times larger an image is than the object. Resolution is the smallest distance between two points that can still be seen as separate. Light microscopes resolve about 200 nm because of the wavelength of light, whereas electron microscopes use electrons with a much shorter wavelength, so they resolve far smaller structures.

Magnification
How many times larger the image is than the real object.
Resolution
The smallest distance between two points at which they can still be seen as two separate points.

Magnification can be increased as much as you like, but the image only shows more detail if the resolution is good enough. Resolution is limited by the wavelength of the radiation used: two points closer together than about half the wavelength merge into one.

magnification = size of image ÷ size of real object
Light and electron microscopes compared
FeatureLight microscopeTransmission electron microscope (TEM)Scanning electron microscope (SEM)
RadiationLight (wavelength about 400 to 700 nm), focused by glass lensesBeam of electrons (very short wavelength), focused by electromagnets, in a vacuumBeam of electrons scanned over the surface, in a vacuum
Maximum useful magnificationAbout ×1500Over ×1 000 000Up to about ×500 000
ResolutionAbout 200 nm (0.2 µm)Roughly 0.1 to 0.5 nmRoughly 3 to 10 nm
SpecimenLiving or dead; thin section or whole mountDead, in a vacuum; extremely thin sectionsDead, in a vacuum; coated with a thin layer of metal
ImageColour (if stained), 2DBlack and white, 2D, shows internal ultrastructureBlack and white, 3D appearance of the surface
ProblemsPoor resolution; cannot see organelle detailPreparation may create artefacts; cannot view living cells; expensiveLower resolution than TEM; surface only

Electron microscopes have a much greater resolution than light microscopes because the wavelength of electrons is much shorter than the wavelength of light. This is why ribosomes, the Golgi apparatus and the inner membranes of mitochondria can only be seen with an electron microscope. Artefacts are structures that appear in the image because of the way the specimen was prepared and are not present in the living cell.

Calculating magnification

A drawing of a cell is 60 mm long. The actual length of the cell is 15 µm. Calculate the magnification of the drawing.

  1. Convert both measurements to the same unit: 60 mm = 60 000 µm.
  2. magnification = size of image ÷ size of real object
  3. magnification = 60 000 ÷ 15

Answer: ×4000

Maths skill:

Write the formula, convert to the same units first, and give no unit for magnification (just ×). To find the actual size, rearrange: actual size = image size ÷ magnification.

Side-by-side diagrams of a light microscope (lamp, condenser lens, specimen on slide, objective lens, eyepiece lens, eye) and a transmission electron microscope (electron gun, electromagnetic condenser, objective and projector lenses, very thin specimen, fluorescent screen, in a vacuum), with bars comparing a resolution of about 200 nm with about 0.5 nm. (opens full size in a new tab)
Electrons have a much shorter wavelength than light, so the TEM has a much higher resolution.

Written and checked against the Edexcel International A Level Biology (YBI11) specification · Updated October 2026

Frequently asked questions

What is the difference between magnification and resolution?

Magnification is how many times bigger the image is than the real object. Resolution is the smallest distance between two points that can still be seen as separate. A higher magnification does not show more detail unless the resolution is also high enough.

Why can an electron microscope show more detail than a light microscope?

An electron microscope uses a beam of electrons, which have a much shorter wavelength than visible light, so it can resolve points a fraction of a nanometre apart. A light microscope resolves only about 200 nm, so cannot show structures such as ribosomes or the inner membranes of mitochondria.

How do you calibrate an eyepiece graticule?

Line up the eyepiece graticule with a stage micrometer of known scale, count how many graticule divisions match a number of micrometer divisions, then divide the known length by the graticule divisions to find the size of one division. Repeat for each objective lens, because the value changes.

All 4 questions on Microscopy and measuring cells