separation of organelles due to their size and mass
Buffer solution has a neutral pH to prevent cells from denaturing.
Buffer solution has same water potential as cell sample to prevent water moving in via osmosis - isotonic solution
Cold temperature to keep organelles from being damaged by enzyme activity
homogenisation of cells using a device in a buffer solution. done to break open cells and allow organelles to escape
a cell homogenate, which is a solution containing organelles found in the cell
filter to remove broken cells, unbroken cells and cell membranes
ultracentrifugation, sample is spun at a low speed at first to separate the heaviest organelle, which experiences a greater force.
After spinning, a nuclei pellet is formed, Th rest of the organelles are suspended in the supernatant
poured into another test tube, spun at a higher speed to separate mitochondria
nucleus, mitochondria, lysosomes, ribosomes
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they may be used on living samples to explore cellular processes
it has the lowest resolution of all other types
the minimum distance between 2 objects where they can still be seen as 2 separate objects
wavelength of light is 400-700nm. If two objects are closer than 200nm, they are not distinguished as two separate objects
image size/ object size
has the highest resolving power of all microscopes
samples must be dead
2d images produced only
electron gun produces a beam of electron which passes down the inside of the microscope, without bouncing off of air molecules. they can be focused using magnets called electromagnetic lenses. sample is placed in path of electron beam. can pass through some sections easier than others
uses beams of electrons to scan sections in a sample. Beam does not pass through the specimen, but instead electrons are scattered from the surface and detected.
generates 3D images
lower resolving power compared to TEM
an incorrect image caused by the stain or microscope