cell structure Flashcards
what are the advantages and disadvantages of using a compound light microscope?
it provides an image in the samples original colour, the sample does not have to be dead when it is being viewed under the microscope, it is also a lot cheaper than an electron, microscope. however due to the wavelength of the light rays it can’t distinguish between objects that are within 0.2 micrometers apart.
how do you calculate magnification?
size of image/size of real object
what is the resolution of a microscope?
the resolution is the minimum distance that two objects can be in order for them to appear as separate items.
what is cell fractionation?
cell fractionation is the process in which a cell is broken up into the different organelles that they contain.
before cell fractionation what must happen to the sample?
it must be placed into a cold, buffered solution with the same water potential as the tissue. it needs to be cold to reduce enzyme activity that may break down the organelles. the water potential needs to be the same to stop the organelles from shrinking or bursting. having a buffer means that the pH won’t fluctuate.
what are the two process of cell fractionation?
homogenisation and ultracentrifugation.
what is the process off ultracentrifugation?
it is the process by which the fragments in the filters homogenate are separated out in a machine called a centrifuge, this spins the homogenate at a very high speed in order to create a centrifugal force.
how is the process of ultracentrifugation carried out for animal cells?
the homogenate is primarily spun at low speeds forcing the heaviest organelles (the nuclei) to the bottom to form a thin sediment, the liquid on top called the supernatant is removed and put back in at a higher speed removing the next heaviest organelles. this process is then continued.
what is the best resolving power of an electron microscope?
0.1nm
what are the two different types of electron microscope?
transmission and scanning.
why can’t the optimum resolution not alwase be achieved on an TEM?
difficulties in preparing the specimen, a higher energy electron beam is required and this may destroy the specimen.
what are the limitations of using an TEM?
the whole thing must be in a vacuum so therefore living specimens can’t be observed; a complex staining process is required and even then the image is not in colour; the specimen must be ultra thin; the specimen may also contain artefacts
what are artefacts?
artefacts are things that result fro the way that the specimen is prepared, there are not part of the natural specimen.
what is the resolving power of an SEM?
it is much lower than that of a TEM of 20nm
how do you calibrate an eyepiece graticule?
you need to use a stage micrometer, this slide has a scale edged onto it. usually the micrometer is 2mm long and has divisions at 1mm intervals.