3.2.1.3 microscopes Flashcards
(18 cards)
resolution
minimum distance between 2 objects where they can still be viewed as seperate
magnification
how many times larger an object is to an image
light microscope advantages and limitations
uses wavelenght of light.
-lower resolution due to longer wavelength of light
-lower magnification
-can be colour
-can be living specimens
light microscope how it works
beam of light condensed by glass lens.
what are the two types of electron microscope
transmittion electron microscope and scanning electron microscope
how TEM works
electron gun shoots beam of electrons at very thin specimen. electrons pass through and areas that absorb appear darker. produces a 2D image
how SEM works
beam of electrons onto surface of specimen. electrons are scattered in different ways to produce a 3D image
advantages and limitations of TEM
-can see internal structures
-2D image
-must be thin
advantages and limitations of SEM
- 3D image
-cant see internal strcutures
-dont have to be thin
advantages and limitations of electron microscope
re condensed by electromagnets
-higher res due to shorter wavelength of electrons
-higher mag
black and white
-must be in vacuum so non-living
equation for magnification
image size= actual x magnification
how to get from mm to micrometers to nanometers
mm–>micrometers= x1000
micrometers–>nanometers= x1000
what is cell fractionation
breaking open cells to release organelles that are then seperated.
why do solutions have to be:
-cold
-isotonic
-buffered
cold: to reduce enzyme activity so organelles arent damaged
-isotonic: prevent osmosis so organelles dont burst
-buffered: keep pH the same to prevent damage to organelles
what is homogenisation
cells are blended in blender to break open cells and release organelles. using cold, isotonic, buffered solution.
solution is filtered to remove any large cell debris
what is ultracentrifugation
solution is spun in centrifugeat different speeds to seperate organelles based on density
what is differential centrifugation
centrifuge is first spun at low speed. most dense organelle will form pellet at bottom of centrifuge. supernatant is collected and centrifuged at increasing speeds and process repeats until all organelles are seperated
what is the order of densities
nucleus, chloroplast, mitochondria, lysosome, ER, ribosome