3.2.1.3 Studying cells Flashcards

1
Q

What is magnification?

A

How many times bigger an object appears

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2
Q

What is resolution?

A

Ability to distinguish two points (how close together two points can be and still be seen as separate points)

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3
Q

How do you calculate magnification from a scale bar or image?

A

Magnification = (image size)/(actual object size)

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4
Q

How do you calculate actual size from an image of known magnification?

A

Actual object size = (image size)/magnification

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5
Q

What is the conversion of 1000µm in 1mm?

A

1000µm = 1mm

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6
Q

What is the conversion of 1000nm in 1µm?

A

1000nm = 1µm

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7
Q

What is the first step in measuring an object using a microscope and graticule?

A

Line up the graticule with the object

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8
Q

What do you do after counting the number of eyepiece units for the measurement?

A

Multiply the number of eyepiece units by the calibration factor

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9
Q

What is the purpose of calibrating the graticule using a stage micrometer?

A

To determine how many µm per eyepiece unit

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10
Q

What is the resolution of optical (light) microscopes?

A

0.2µm

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11
Q

What is the magnification range of optical (light) microscopes?

A

x2000 - x1500

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12
Q

How do optical (light) microscopes work?

A

Light waves are focussed onto an object, and then onto the eye, using glass lenses

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13
Q

What are some uses of optical (light) microscopes?

A

Study living and dead cells; cells can be stained to see features more easily

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14
Q

What are the limitations of optical (light) microscopes?

A

Relatively low magnification and resolution, cannot see all organelles in a cell

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15
Q

What is the resolution of a transmission electron microscope (TEM)?

A

0.1nm

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16
Q

What is the magnification of a transmission electron microscope (TEM)?

A

x50 000 000

17
Q

How does a transmission electron microscope (TEM) work?

A

Beams of negatively charged electrons are focused using electromagnets and pass through the cell

18
Q

What are the uses of a transmission electron microscope (TEM)?

A

View ultrastructure of cells (all organelles can be visualised)

19
Q

What are some limitations of a transmission electron microscope (TEM)?

A
  • Vacuum required for microscope to function
  • Specimen must be very thin
  • Staining with metals required
  • Cells must be dead
  • Artefacts may occur
20
Q

What is the resolution of a scanning electron microscope (SEM)?

21
Q

What is the magnification of a scanning electron microscope (SEM)?

A

x1 000 000

22
Q

How does a scanning electron microscope (SEM) work?

A

Beams of negatively charged electrons are focused using electromagnets and reflect off the surface of an object

23
Q

What are the uses of a scanning electron microscope (SEM)?

A

Beam is scanned across the surface, allowing a 3-D image to be built up

24
Q

What are some limitations of a scanning electron microscope (SEM)?

A
  • Vacuum required for microscope to function
  • Specimen must be very thin
  • Staining with metals required
  • Cells must be dead
  • Artefacts may occur
25
What is homogenation in the context of extracting organelles for study?
Cells are kept in a solution that is pH buffered, cold, and isotonic
26
What does the solution used in homogenation prevent?
* Denaturation of proteins * Digestion of organelles * Water movement into organelles by osmosis
27
What is the first step in the ultracentrifugation process?
The tube of homogenate is placed in a centrifuge and spun at low speeds
28
What settles at the bottom of the tube during the first spin in ultracentrifugation?
The heaviest organelles, the nuclei
29
What is done with the supernatant in ultracentrifugation?
It is removed, placed in a new tube, and spun at higher speeds
30
What settles at the bottom of the tube during the subsequent spins in ultracentrifugation?
The next heaviest organelles, such as mitochondria or chloroplasts
31
What is repeated several times in the ultracentrifugation process?
The process of removing the supernatant to a new tube and spinning at higher speeds