Microscopy and Magnification
Magnification ; convert to the same unit first (1 mm = 1000 µm; 1 µm = 1000 nm). Resolution is the ability to distinguish two close points: light microscopes resolve about 200 nm; electron microscopes about 0.5 nm because electrons have a much shorter wavelength. TEM gives 2D sections with internal detail; SEM gives 3D surface images; both need a vacuum, so specimens are dead. An eyepiece graticule is calibrated against a stage micrometer (divisions of known size, often 10 µm) at each objective. Cell fractionation: homogenise in cold, isotonic, buffered solution, then ultracentrifuge: nuclei sediment first, then mitochondria, then ribosomes.
Learning objectives
- Use the magnification equation with unit conversions.
- Calibrate an eyepiece graticule.
- Distinguish magnification and resolution.
- Compare light, TEM and SEM; describe cell fractionation.
If you enlarge a blurry photo, you don't see more detail. What does that say about magnification versus resolution?
Core idea
Zoom into a phone photo and it just gets blurry. Microscopes have the same limit: resolution.
Magnification is image size ÷ actual size. Resolution, set by wavelength, decides how much detail you can see.
- Each stage division is 10 µm.
- Line up the scales and count eyepiece units.
- Divide.
An image is 36 mm long; the cell is 12 µm. Magnification?
- Goal
- M.
- Strategy
- Convert to µm, then divide.
- ×1000.
- Image ÷ actual.
Trade-offs between detail and living specimens.
Summary
- M = I / A.
- Calibrate graticule.
- Resolution limited by wavelength.
- Resolution
- Minimum distance between two points that can be seen as separate.
- Stage micrometer
- Slide with a scale of known divisions.
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