Cell Structure Flashcards
what is the formula for finding the size of a cell
magnification=size of image/size of real object
what is the comman unit of cell study
micrometer
micrometer is
x10-6
how do you convert between units
1mm x1000 = 1000 micrometers
1000 micrometers x1000= 1000000 nano
1mm x1000000= 1000000 nm
magnification
how many times bigger the image is compared to the object
resolution
the ability to distinguish between two separate points
the resolution depends on
the wavelength of the radiation source
2 examples of radiation
-light ray
-electron beam
what makes the image clearer
being hit by two waves of radiation
what makes up a light microscope
- condenser lens- focuses light up onto the stage
- the specimen - the thing you want to view
- objective lens - magnifies the specimen
- eyepiece lens - magnifies image further
how is total magnification achieved
by multiplying mag of both lenses together
how are different shades produced
different parts of specimen have different densities
therefore parts of the specimen absorbs different amounts of wavelength
what is the total magnification of a light microscope
x1500
what is the total resolution of a light microscope
0.2 micrometers
advantages of light
-cheap and easy to maintain
- easy to prepare specimens, can use a stain
- living specimens can be used
disadvantages of light
-limited magnification
-low resolution
when were electron microscopes invented
1930 , not used until 1950
when was the light microscope invented
1667 - robert hooke
types of microscope
transmission electron microscope
scanning “”
advantages of electron
-high resolution
-high magnification
what is the magnification of an electron
x250000
disadvantages of electron
-only dead specimens can be viewed
-cannot use harsh stains
- expensive
-have to have special training
what is an artefact
features that are caused by preparation and do not really exist in the cell
how do you combat artefacts
ask other scientists to see if they see what you see
why do electron microscopes have to be in a vacuum
the electrons are too small and can scatter easily
how do you prepare specimens for electron
cut extremely thin using a diamond knife
how do TEMs work
-electron beams are emitted by an electron gun
-they are then narrowed by electromagnetic lenses onto the specimen
-electrons penetrate through the specimen
-different areas appear dark and light due to the levels of electrons that they absorb (electron densities)
how do SEMs work
-electrons fired out of a gun
-narrowed by electromagnetic lenses
-scan over the top ad under the specimen, instead of going through
what is an advantage of scanning
3D images can be produced
how do you measure cells
using an eyepiece graticule and stage micrometer
what is an eyepiece graticule
-small glass disc that is placed in the eyepiece lens
-usually divided into 100 units
how do you chose the correct setting for the eyepiece
calibrate it against a known length
how do you calibrate it
using the stage micrometer
what is the typical length of stage micrometer
1mm divided into 100 divisions therefore each one is usually 10 micrometers
example
each division is 10 micrometers
24 divisions line up with 90 on the eyepiece graticule
24x10= 240 micrometers
240=90
240/90 = each eyepiece division is 2.67 micrometers
what do you have to do each time you change the magnification
you have to re-calibrate it
what do you have to do before each calculation
line both EPG and SM up to closet lines and count distance between