Module 2.1 Cell Structure Flashcards
Magnification🔎
How much bigger an image appears compared with the original object
Resolution
The ability to be able to distinguish between 2 points that are very close together
Advantages of light microscopes🔬
Relatively cheap, easy to use, portable, can study living specimens
Max magnification of a light microscope 🔬
1500 times
Max resolution of a light 🔬
200nm
How do you calculate total magnification
Magnifying power of the objective lens TIMES BY magnifying power of the eyepiece lens
Disadvantages of electron microscopes
Large, expensive, needs a great deal of skill and training to use, specimens need to be dead
Image formed by transmission electron microscopes
2D Black and White image
Image formed by scanning electron microscope
3D Black and White (although false colour can be added)
Acetic oncein binds to DNA and stains chromosomes
Dark red🌶👹👺💃🏿🎒🦀🍎🍒🍷
Name an example of an all purpose stain
Methylene blue 💤🐟💦👖👕🐳🐬☄️🎽🚙🛢
How would you prepare a specimen?
Dehydrate the specimen, embed it in wax (to prevent distortion) and section the specimen
Calculations involving magnification formula
Magnification = Image DIVIDED BY Actual size
Features of a generalised animal cell
Ribosomes Mitochondria Nucleolus Nucleus Smooth Endoplasmic Reticulum Plasma membrane Golgi apparatus Lysosomes Nuclear envelope Rough Endoplasmic Reticulum
Features of a generalised plant cell 🌱
Chloroplast Amyloplast containing starch Golgi apparatus Smooth Endoplasmic Reticulum Ribosomes Nucleolus Nucleus Nuclear envelope Rough Endoplasmic Reticulum Plasma membrane Cell wall Vacuole Mitochondria
🌟Describe the stages in the production of extracellular proteins
- mRNA copy of the gene is made in the nucleus 〰 (transcription)
- mRNA leaves the nucleus through a nuclear pore
- mRNA attaches to a ribosome (e.g. attached to the rough endoplasmic reticulum). The ribosome reads the instructions to assemble a protein (translation)
- Molecules are “pinched off” in vesicles and travel towards the Golgi apparatus
- Vesicle fuses with the Golgi apparatus
- Golgi apparatus processes and packages 📦 the molecules ready for release
- Packaged molecules 📦are “pinched off” in vesicles from Golgi apparatus and move towards the plasma membrane
- Vesicle fuses with the plasma membrane
- Protein released out of the cell by exocytosis
Light microscopes can be used to observe dead specimens? True or false
False
Light microscopes can be used to observe tissue in colour? True or false
True
Light microscopes can be used to observe organelles of cells? True or false
True
Light microscopes can be used to observe the movement of cells? True or false
True
What features of a 🌱 cell would you expect to be able to see under a light microscope?
The cell wall, the nucleus, the cytoplasm and the chloroplasts
Explain why you can only see limited organelle when looking at a 🌱cell under a light microscope
The resolution of a light microscope is 200nm and the max magnification is 1500 times. The magnification and resolution are too low to observe most organelle of the cell.
Scanning electron microscopes can be used to observe 2D images, true or false?
False
Scanning electron microscopes can be used to observe cell surfaces, true or false?
True
Scanning electron microscopes can be used to observe cells in colour, true or false?
False
Scanning electron microscopes can be used to observe cells in real time, true or false?
False
Strengths and weaknesses of light and electron microscopes
Light microscopes strengths:
Cheap, portable, easy to use, can study living or dead specimens with them
Light microscopes weaknesses:
Limited resolution and magnification, most organelles are too small to see at this power
Electron microscopes strengths:
High magnification and resolution
Electron microscopes weaknesses:
Large, needs skills and training to operate, specimen must be dead
Which of these statements are true?
1) Stains can be used to distinguish between different cell types
2) Stains can be used to fix specimens
3) Stains can be used to distinguish different tissue types
4) Stains can be used to highlight particular organelle
1, 3 and 4 only
How would you prepare a temporary mount of a specimen for a light microscope?
Section the specimen, put it on a slide, stain it, put a coverslip over the specimen
How would you calculate magnification?
Image size divided by actual size
How would you calculate the image size?
Actual size times by magnification
How would you calculate the actual size of a cell?
Image size divided by magnification
Organelle present in animal cells
Nucleolus Nucleus RER SER Ribosomes Mitochondria Golgi apparatus Centrioles Plasma membrane Cytoskeleton