2.1.1 Cell structure Flashcards
(47 cards)
What is magnification?
Magnification is how many times larger an image is than the actual object.
What is resolution?
Resolution is the ability to distinguish between two separate points
It determines how detailed an image is.
What is the formula for calculating magnification?
-
What is an eyepiece graticule used for?
A scale fitted into the eyepiece used to measure objects under the microscope, but it must be calibrated for accuracy.
What is a stage micrometer used for?
A slide placed on the stage with a known scale (in µm) used to calibrate the eyepiece graticule.
How do you calculate the size of one graticule division?
Graticuledivision= Numberofgraticuledivisions ÷
Sizeofonemicrometerdivision
If 40 graticule divisions = 1 micrometer division (10 µm), what is the size of one graticule division?
0.25 μm
Name four types of microscopes.
- Light microscope
- Transmission electron microscope (TEM)
- Scanning electron microscope (SEM)
- Laser scanning confocal microscopes
What are the resolution and magnification limits of a light microscope?
Resolution: ~0.2 µm
Magnification: up to x1,500
What are four slide preparation techniques?
- Wet mounts
- Dry mounts - Specimen is placed directly onto slide and covered with a cover slip.
- Squash slides - A wet mount is prepared and the cover slip is pressed to squash the cells.
- Smear slides - Edge of a slight is used to smear the sample to create a thin, even coating on a seperate slide.
What are the steps for preparing a wet mount slide?
- Use a pipette to place a small drop of water onto the centre of the glass slide.
- Use a pair of forceps to place a thin section of the live specimen onto the drop of water. The specimen should be thin enough to allow light to pass through it.
- Add a few drops of stain to the specimen - increases contrast & allows cell components to become visible.
- Slowly add a cover slip onto the specimen
Viola✨
Why is differential staining used?
It uses multiple stains to distinguish between different cells or organelles.
What are the basic steps to view a slide under a light microscope?
- Clip the prepared microscope slide onto the stage.
- Select objective lens with lowest power
- Use coarse focus to bring stage up.
- Look through eyepiece and slowly lower stage to focus, using coarse focus.
- Use fine focus for a clear image.
- ncrease magnification if needed and refocus.
What are the key features of a good biological drawing?
Include a title
State magnifications or scale
Be drawn with a sharp pencil
Include smooth, continuous lines
Include labels
Include accurate sizes of observable features
No shading ot colouring
No arrow heads
Lines cannot overlap each other.
How does an electron microscope differ from a light microscope?
It uses a beam of electrons (instead of light) to form an image, providing much higher resolution and magnification.
What are the advantages and disadvantages of electron microscopes?
✅ Higher resolution and magnification
❌ Expensive
❌ Only black and white images
❌ Complex sample preparation
❌ Can only be used on dead specimens
What are the two types of electron microscopes?
- Transmission electron microscope (TEM)
- Scanning electron microscope (SEM)
What are the resolution and magnification limits of a TEM?
Resolution: ~0.5 nm
Magnification: up to ×1,500,000
How does an SEM work and what does it show?
It scans electrons across the specimen’s surface.
Reflected electrons form a 3D image of the surface.
What are the resolution and magnification limits of an SEM?
Resolution: ~5 nm
Magnification: up to ×1,500,000
How do light, TEM, and SEM microscopes compare?
Light: Mag = ×1,500 & Res = 0.2 µm, inexpensive, 2D image, colour, specimen can be living or dead
TEM: Mag = ×1,500,000 & Res = 0.5 nm, expensive, 2D image, B&W, specimens are dead
SEM: Mag = ×1,500,000 & Res = 5 nm, expensive, 3D image, B&W, specimens are dead.
Describe how a laser scanning confocal microscope works.
- Uses a laser beam to scan across a specimen that has been treated with a fluorescent dye.
- The laser excites the dye, causing it to emit light (fluorescence).
- This produces a high-resolution, sharp 2D image — multiple images at different depths can be combined to create a 3D image.
What are the two main types of organisms based on cell structure?
Eukaryotes
Prokaryotes
What is the main difference between eukaryotic and prokaryotic cells?
- Eukaryotic cells are more complex, contain membrane-bound organlles, have 80s chromosomes and have their DNA in the form of chromosome within the nucleus.
- Prokaryotes contain no membrane-bound organelles (no mitochondria or chloroplasts), have 70s ribsomes and have circular naked DNA with no nucleus.