Differences in microscopes (Simplified version)
DIFFERENCES
IN MICROSCOPES
Features |
Compound microscope |
Phase – contrast
microscopes |
Fluorescence
microscopes |
Electron microscopes |
Scanning acoustic
microscope |
Source |
Natural light/
Artificial light |
Artificial light
source |
UV Light, LASER |
Electron source |
Sound waves |
Types |
1. Bright Field 2. Dark Field |
1. Phase contrast 2. Differential
interference contrast |
1. Fluorescence 2. Confocal laser
scanning 3. Two-photon microscope
|
1. Scanning electron 2. Transmission electron
|
1. Scanning acoustic
microscope |
Cells viewed |
Stained, unstained
live cells |
Unstained live cells |
Stained, live cells |
Stained, killed cells |
Unstained |
Images |
Coloured (Bright
field), contrast images (dark
field) |
Dark contrast images |
Coloured images |
Black and white
images, 2D and 3D images |
Graphical represented
images |
Condenser |
Bright field; Dark field |
Phase contrast
condenser with annular stop. DIC – two Wollaston
prisms |
Filters: 1. Exciter filter 2.
Barrier filter 3.
Dichroic mirror Confocal: Pinhole apertures |
Electromagnetic coils
|
|
Smear preparation |
Thin |
Thin |
Thin; thick for Two photon |
Thin for TEM Thick for SEM |
Thick and thin |
Stains used |
Acids and bases |
No stain |
Fluorochromes |
Metals |
Water as a medium |
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