AQA A Level Chemistry: Methods of Studying Cells Flashcards
What are the three main types of microscopes used to study cells?
- Light microscope
- Transmission electron microscope (TEM)
- Scanning electron microscope (SEM)
What is magnification?
magnification= size of image/ actual size of object
What is resolution?
The ability to distinguish two objects as separate entities; higher resolution gives a clearer and more detailed image.
What is the maximum magnification and resolution of a light microscope?
- Magnification: x1500
- Resolution: 200 nm
How does a transmission electron microscope (TEM) work?
- Passes a beam of electrons through a thin specimen.
- Denser areas absorb more electrons, appearing darker.
- Produces 2D images with very high resolution.
What is the maximum magnification and resolution of a TEM?
- Magnification: x1,000,000
- Resolution: 0.1 nm
How does a scanning electron microscope (SEM) work?
- Beams electrons across the surface of the specimen.
- Reflected electrons create a 3D image of the surface.
What is the maximum magnification and resolution of a SEM?
- Magnification: x500,000
- Resolution: 1–20 nm
What are the advantages of using a light microscope?
- Can observe living cells.
- Easy to use and prepare slides.
- Produces colour images.
What are the limitations of a light microscope?
- Low resolution and magnification.
- Cannot see internal organelles in detail.
What are the advantages of a TEM?
- High resolution shows detailed internal structures.
- Can see organelles like ribosomes and membranes.
What are the limitations of a TEM?
- Only produces 2D images.
- Requires thin specimens.
- Can only view dead specimens due to vacuum.
What are the advantages of a SEM?
- Produces detailed 3D images of the surface.
- Good for studying external structures.
What are the limitations of a SEM?
- Lower resolution than TEM.
- Can only view dead specimens.
What is cell fractionation?
A process used to separate organelles from cells to study their structure and function.
What are the three main steps of cell fractionation?
- Homogenisation – Breaking cells open using a blender.
- Filtration – Removing debris and whole cells.
- Ultracentrifugation – Spinning at high speeds to separate organelles by density.
What are the conditions for cell fractionation?
- Cold: Reduces enzyme activity.
- Isotonic: Prevents osmosis and organelle damage.
- Buffered: Maintains pH to avoid denaturing enzymes.
What is the order of organelles separated by ultracentrifugation?
- Nucleus (heaviest)
- Chloroplasts (in plant cells)
- Mitochondria
- Lysosomes
- Endoplasmic reticulum
- Ribosomes (lightest)
What is the pellet and supernatant in ultracentrifugation?
- Pellet: Contains the denser organelles that settle at the bottom.
- Supernatant: The liquid above containing lighter organelles.
What is artefact formation in electron microscopy?
Structures that appear due to sample preparation, not actually part of the specimen.