M3: Microscopy Flashcards
Micrometer (Mm)
one millionth of meter (10^-6 m)
nanometer (mm)
one billionth of meter (10^-9 m)
resolution
- distance between two objects at which they can still be seen as separate
- objects that are closer to each other will require a higher resolution to be seen as separate
contrast
- difference in light absorbance between 2 objects
- lower contrast –> harder to see object
brightfield microscopes overview
- simplest kind of light microscope
- can only reach resolutions of up to 0.3 Mm –> can’t visualize viruses
how brightfield microscopes work (5 steps)
- light (halogen bulb usually) enters microscope from base
- mirrors reflect light towards sample
- before light reaches sample, it passes through condenser (converges light beams into focused area on sample)
- once light passes through sample, iris diaphragm controls how much of that light enters the objective lens (closest lens to sample, highest amount of magnification)
- light passes through objective lens –> ocular lens (eyepiece) –> eye
total magnification
magnification of objective lens x magnification of ocular lens
typical magnification of ocular lens
10x
phase contrast microscope overview
- uses special condensers and objectives to amplify small differences between cell and background –> can obtain detailed images of specimens without needing to stain samples (so can visualize movement)
- sometimes will dye specific parts of a cell to highlight something
dark field microscope overview
- greatly increases contrast, resulting in a dark background and bright objects as light reflects off of specimen
- can’t see inside cells using this method
- often used to find lyme disease pathogen
fluorescence microscope overview
- uses fluorophores to see cells on a dark background
- how it works: emits wavelengths to excite fluorophores into producing different colors
fluorophores
- fluorescent molecules
- colors most used = green (GFP), yellow (YFP) , and red (RFP)
uses of fluorophores in microscopy (3)
- illuminate cells as a whole
- couple with normal cellular protein to visualize protein movement and localization
- tag molecules or antibodies to ID the presence (or absence) of particular proteins
confocal microscope overview
- aka laser-scanning microscope
- uses lasers to focus on single place within an object, which increases accuracy of the visualization
- then compiles these images into a single 2D or 3D image
electron microscopes overview
- use electron beams instead of light beams
- electron beams have shorter wave lengths –> increased resolution capacity ( >1nm) –> used to visualize super small specimens
- labor intensive process, samples must be fixed
- 3 types: TEM, SEM, STEHM