The quality of an image under the light microscope depends on:
Three lenses in a compound microscope
Magnification
The product of the individual magnifications of the ocular and objective lenses
Condenser lense function
Focuses the light on the specimen
What minimum magnification is needed to view cells
100 x
Resolving power (d)
The ability of a lens system to allow you to see two points as being distinct
Do higher or lower values of ‘d’ mean greater resolution
Lower
Resolution formula
-d = wavelength/ (2 NA) N = refractive index of space between specimen & lens A = numerical aperture
Resolving power can be maximized by:
- Use a shorter wavelength of light
Oil immersion
The refractive index of oil is much closer to that of glass
- Capture more refracted light
Brightfield
Dark objects are visible against a bright background
Darkfield
Light objects are visible against a dark
Fluorescence Microscopy
Adhere fluorescent dyes to the specimen
- Fluorescent substances absorb u.v. light, and emit visible light
Confocal Microscopy
Short wavelength light progressively focused at different depths of dyed specimen
- Produces 3-dimensional image
Electron Microscopy
Similar to brightfield except that an electron beam is used rather than visible light
TEM (Transmission Electron Microscopy)
Electron beam passes through specimen then an electromagnetic lens, to a screen/film
- Embedded in special resin
SEM (Scanning Electron Microscopy)
Electron beams knocks other electrons off the surface of a specimen
Simple Stains
What overall charge do bacteria have?
Negative
What charge do chromophores have?
Positive
Examples of basic dyes
Crystal violet & safranin
Negative (acidic) Stains
Differential Stains
Use simple stains in different ways to visualize specific structure and features of the specimen
- Use mordants & counterstains
Mordants
Chemicals to modify and enhance the action of the simple stain