Cells: Methods of studying cells Flashcards

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1
Q

What type of microscope would be used to see a living water flea specimen? Why?

A
  • Optical microscope
  • Specimen has to be living
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2
Q

What type of microscope would be used to see a pollen grain surface? Why?

A
  • Scanning electron microscope
  • Provides a 3D scan of the surface
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3
Q

What type of microscope would be used to view cristae in a mitochondrion? Why?

A
  • Transmission electron microscope
  • High resolution allows detail to be seen
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4
Q

What type of microscope would be used to view the stages of mitosis in a root cell? Why?

A
  • Optical microscope
  • Sample needs to be alive
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5
Q

What are the three types of microscopes?

A
  • Optical microscope
  • Scanning electron microscope
  • Transmission electron microscope
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6
Q

What is the equation for mitotic index?

A

Mitotic index = Cells in mitosis / Total number of cells

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7
Q

What is the equation for magnification?

A

Magnification = size of image/size of real object

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8
Q

How do you convert mm (millimetre) into um (micrometre)?

A

x 1000

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9
Q

How do you convert um (micrometre) into nm (nanometre)?

A

x 1000

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10
Q

Give the three microscopic units in order of their size:

A

Millimetre (mm)
Micrometre (um)
Nanometre (nm)

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11
Q

How do you convert nanometre (nm) into micrometre (um)?

A

/ 1000

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12
Q

How do you convert micrometre (um) into milimetre (mm)?

A

/ 1000

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13
Q

Define resolution:

A

How detailed an image is.

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14
Q

How do transmission electron microscopes work?

A

Use electromagnets to focus a beam of electrons, which is then transmitted through the specimen.

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15
Q

Why do denser parts of a specimen appear darker through transmission electron microscopes?

A

Denser parts of the specimen absorb more electrons.

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16
Q

Give 1 advantage of TEM:

A

High resolution = so shows small objects

17
Q

Give 2 disadvantages of TEM:

A
  • Can only be used on thin specimens
  • Can only be used on non-living specimens
18
Q

Give 2 advantages of SEM:

A
  • Can be used on thick specimens
  • Can produce a 3D image
19
Q

Give 2 disadvantages of SEM:

A
  • Lower resolution than TEM
  • Can only be used on non-living specimens
20
Q

What are the three steps of cell fractionation?

A

1) Homogenisation
2) Filtration
3) Ultracentrifugation

21
Q

What is the purpose of homogenisation in cell fractionation?

A

Breaks up plasma membrane and releases organelles into solution.

22
Q

Why must the solution be kept ice-cold?

A

Prevent enzyme activity

23
Q

Why must the solution be isotonic?

A

So the concentration of chemicals in the solution and organelles are same, to prevent the organelles being damaged.

24
Q

Why must the solution contain a buffer?

A

To maintain the pH.

25
Q

Explain the first step of cell fractionation, homogenisation:

A

1) Cell is broken up (e.g. in a blender) so plasma membrane is broken up.
2) Organelles are released into an ice-cold, isotonic, buffer solution.

26
Q

Explain the second step of cell fractionation, filtration:

A

1) Homogenised cell solution is filtered through gauze to remove debris.

27
Q

Explain the third step of cell fractionation, ultracentrifugation:

A

1) Cell fragments are poured into a tube. Tube is put into a centrifuge and is spun at a low speed.
2) Densest organelles (e.g. nuclei) sink first forming pellets and are removed.
3) Tube is spun again at a higher speed - process is repeated.