AQA A Level Chemistry: Methods of Studying Cells Flashcards

1
Q

What are the three main types of microscopes used to study cells?

A
  1. Light microscope
    1. Transmission electron microscope (TEM)
    2. Scanning electron microscope (SEM)
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2
Q

What is magnification?

A

magnification= size of image/ actual size of object

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3
Q

What is resolution?

A

The ability to distinguish two objects as separate entities; higher resolution gives a clearer and more detailed image.

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4
Q

What is the maximum magnification and resolution of a light microscope?

A
  • Magnification: x1500
    • Resolution: 200 nm
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5
Q

How does a transmission electron microscope (TEM) work?

A
  • Passes a beam of electrons through a thin specimen.
    • Denser areas absorb more electrons, appearing darker.
    • Produces 2D images with very high resolution.
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6
Q

What is the maximum magnification and resolution of a TEM?

A
  • Magnification: x1,000,000
    • Resolution: 0.1 nm
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7
Q

How does a scanning electron microscope (SEM) work?

A
  • Beams electrons across the surface of the specimen.
    • Reflected electrons create a 3D image of the surface.
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8
Q

What is the maximum magnification and resolution of a SEM?

A
  • Magnification: x500,000
    • Resolution: 1–20 nm
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9
Q

What are the advantages of using a light microscope?

A
  • Can observe living cells.
    • Easy to use and prepare slides.
    • Produces colour images.
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10
Q

What are the limitations of a light microscope?

A
  • Low resolution and magnification.
    • Cannot see internal organelles in detail.
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11
Q

What are the advantages of a TEM?

A
  • High resolution shows detailed internal structures.
    • Can see organelles like ribosomes and membranes.
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12
Q

What are the limitations of a TEM?

A
  • Only produces 2D images.
    • Requires thin specimens.
    • Can only view dead specimens due to vacuum.
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13
Q

What are the advantages of a SEM?

A
  • Produces detailed 3D images of the surface.
    • Good for studying external structures.
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14
Q

What are the limitations of a SEM?

A
  • Lower resolution than TEM.
    • Can only view dead specimens.
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15
Q

What is cell fractionation?

A

A process used to separate organelles from cells to study their structure and function.

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16
Q

What are the three main steps of cell fractionation?

A
  1. Homogenisation – Breaking cells open using a blender.
    1. Filtration – Removing debris and whole cells.
    2. Ultracentrifugation – Spinning at high speeds to separate organelles by density.
17
Q

What are the conditions for cell fractionation?

A
  • Cold: Reduces enzyme activity.
    • Isotonic: Prevents osmosis and organelle damage.
    • Buffered: Maintains pH to avoid denaturing enzymes.
18
Q

What is the order of organelles separated by ultracentrifugation?

A
  1. Nucleus (heaviest)
    1. Chloroplasts (in plant cells)
    2. Mitochondria
    3. Lysosomes
    4. Endoplasmic reticulum
    5. Ribosomes (lightest)
19
Q

What is the pellet and supernatant in ultracentrifugation?

A
  • Pellet: Contains the denser organelles that settle at the bottom.
    • Supernatant: The liquid above containing lighter organelles.
20
Q

What is artefact formation in electron microscopy?

A

Structures that appear due to sample preparation, not actually part of the specimen.