2.1.1 cell structure Flashcards
what is the magnification of a light microscope
2.1.1(a)
2000x
what is the resolution of a light microscope
2.1.1(a)
200nm
how do light microscopes work
2.1.1(a)
they use visible light to illuminate the specimen
what is the resolution of a light microscope limited by
2.1.1(a)
the wavelength of visible light
what is the magnification of a laser scanning confocal microscope
2.1.1(a)
1000x
what is the resolution of a laser scanning confocal microscope
2.1.1(a)
120nm
how does laser scanning confocal microscopy produce an image/what colour
2.1.1(a)
it uses a laser and a concentrated beam of light to scan an object point by point
the information is assembled by a computer into one image and displayed on a computer screen
the colour of fluorescent tag which glow a certain colour under the UV laser light
what cells can laser scanning confocal microscopy be used on and what does it show
2.1.1(a)
used on live cells
so an image can be taken every few seconds to show the movement of substances inside cells
what is the magnification of TEM
2.1.1(a)
2 000 000x
what is the resolution of TEM
2.1.1(a)
1nm
how do TEM produce an image and what is that image called
2.1.1(a)
they use a beam of electrons to illuminate the specimen
the image is then interpreted by a computer
it is called an electron micrograph
what cells are TEM used on and why
2.1.1(a)
dead cells
the specimen has to be sliced thinly then fixed using a highly toxic stain
AND
the sample must be placed in a vacuum so that electrons in the beam aren’t scattered by air particles
what colour is the image produced by TEM 2.1.1(a)
black and white until artificial false colour is added
what is the magnification of a SEN
2.1.1(a)
200 000x
what is the resolution of a SEN
2.1.1(a)
20nm
How is an image assembled by a computer using a SEN
2.1.1(a)
the sample is sprayed with a fine film of metal atoms
electrons are scattered from the metal atom layer and detected by an electron detector
the image is assembled by a computer
What colour is the image assembled by an SEN
2.1.1(a)
black and white until artificial false colour is added
is the image produced by a laser scanning confocal microscope 2D or 3D
2.1.1(a)
3D
is the image produced by a TEM 2D or 3D
2.1.1(a)
2D
is the image produced by a SEM 2D or 3D
2.1.1(a)
3D
How do you prepare a dry mount slide
2.1.1(b)
solid specimens are used whole or cut into very thin slices with a sharp blade or a microtome
a specimen is then placed on a slide
a coverslip may be used to keep the specimen in place
what samples are suitable a dry mount slide
2.1.1(b)
pollen, hair, feathers and parts of insects
How do you prepare a wet mount
2.1.1(b)
samples are suspended in liquid eg-water or immersion oil
a coverslip is placed at an angle to prevent air bubbles
living cells or small organisms can be viewed this way as the liquid allows them to live and move
how to prepare a squash slide and example
2.1.1(b)
a wet mount is prepared then a lens tissue is used to gently press down the coverslip
this flattens out a soft sample
for example a squash at the tip of a garlic root is often used to examine cell division
how can you minimise damage to the coverslip on the squash slide
2.1.1(b)
by squashing the sample between two microscope slides
what is a transverse section AKA cross-section
2.1.1(b)
where a cut is made perpendicular to the long axis of a structure
what is a longitudinal section
2.1.1(b)
where a cut is made parallel to the long axis of a structure
What is an eyepiece graticule
2.1.1(b)
a scale embedded in the eyepiece that does not have any measurements on it
what is a stage micrometer
2.1.1(b)
a stage micrometer is used to calibrate the eyepiece graticule
how do you calibrate the eyepiece graticule
2.1.1(b)
- Focus on stage micrometer using the desired objective lens
- move the eyepiece graticule and the stage micrometer until they line up
- count how many stage micrometer divisions fit inside a certain number of eyepiece graticule divisions
What is differential staining and when is it useful
2.1.1(c)
staining process that uses more than one stain
its useful when looking at blood smears-its useful to have WBC and RBC different colours to make it easier to see and identify them
what does methylene blue bind to
2.1.1(c)
DNA stains it blue
what does crystal violet bind to
2.1.1(c)
pedtidoglycan
what is gram staining
2.1.1(c)
staining procedure used to classify bacterial species
gram + and gram - bacteria have different cell wall structures so different antibiotics are effective for each group
we can therefore see which bacteria a patient is effected with
describe or draw the structure of gram positive bacteria
2.1.1(c)
-thick peptidoglycan layer
-with NO outer lipopolysaccharide membrane
-they have a cytoplasmic membrane at the bottom
describe or draw the structure of gram negative bacteria
2.1.1(c)
-DOES have an outer lipopolysaccharide layer
-has a THIN peptidoglycan layer
-also has a cytoplasmic membrane
describe the steps involved in staining bacterial colonies
2.1.1(c)
- cells are stained with crystal violet which binds to peptidoglycan so all cells turn purple
2.iodine solution is added which forms a complex with the crystal violet stain and traps it within the cell
3.the cells are washed with ethanol which decolourises the gram - bacteria as it dissolves the outer lipopolysaccharide membrane so the crystal violet washes out
4.gram - cells are visualised by applying a pink coloured counterstain called safranin. Both cells retain the counterstain BUT the pink colour cannot be distinguished in the purple stained gram + cells