cell structure Flashcards
(41 cards)
what is magnification
the number of times larger an image appears, compared with the size of the object being viewed
what is resolution
how clearly we can determine two points, the higher the resolution the greater the detail
what is wet mounting
specimens are suspended in a liquid such as water or immersion oil
what is dry mounting
solid specimens are viewed whole or cut into very thin slices
why must we place a cover slip on at an angle (when placing it onto a wet mount)
this is to prevent air bubbles forming under the cover slip
what is the maximum magnification and resolution of a scanning electron microscope (SEM)
- 15 to 200,000 times (magnification range)
- 3-10 Nm (resolution range
what is the maximum magnification and resolution of a transition electron microscope (TEM)
- x 2 million (magnification range)
- 0.5nm (resolution range)
what are the disadvantages of electron microscopes
- the specimen has to be chemically fixed, by being dehydrated and stained
- vacuum required
- large and needs to be installed
- expensive to buy/operate
- specimens must be dead
what is the function of the mitochondrion
mean length = 0.5 to 1 um
- to produce energy in respiration
what is the function of chloroplasts
mean length = 3-10 um
uses light energy in photosynthesis
- convert light energy in to stable chemical energy
what is the function of the Golgi apparatus
mean length = 0.5 to 2.0 um
to function as a factory in which proteins are processed and transported to the plasma membrane etc.
what is the function of the smooth ER
mean length =30nm to 50nm
it synthesis and stores lipids including cholesterol and phospholipids to produce new cellular membranes
what is the function of the rough ER
mean length = 20nm to 30nm
to produce proteins that will become part of the Endomembrane system, the plasma or will be secreted
(the endomembrane systems is all of the membranes within the cell)
what are centrioles
- centrioles, move to the poles (opposite ends of the cell) of the cell
- froms spindle fibres, which often attach to chromosomes
what are flagella
- flagella are prokaryotes/ bacteria
- ## whip like movement
what are cilia
- same structure as the flagella, but shorter
- beating movement
- arranged in clusters
what are microfilaments
- filaments found in the cytoplasm
- help the cell move
- change shape (endocytosis and exocytosis)
what are microtubles
- little tubes (microscopic)
- form the spindle
- make up cilia and undulipodia, so help, with the movement of substances
- motor proteins, allow them to move via ATP
what are intermediate fibres
- extended between cells and help to stabilise the tissue
what are lysosomes
- Specialist forms of vesicles which contain hydrolytic enzymes (enzymes that break biological molecules down)
- Break down waste materials such as worn-out organelles, used extensively by cells of the immune system and in apoptosis (programmed cell death)
State some advantages and disadvantages of light microscopes
easy to use, portable, can be used to observe living specimens (tissues) DISADS: Limited magnification and resolution so fine detail cannot be observed
State the maximum magnification and resolution for a light microscope
M = 1500 - 2000 times; R = 200nm (0.2µm)
Describe reasons why we use staining in microscopy
Coloured chemicals that bind to molecules on the specimen, increasing contrast and making the specimen easier to see; some stains bind to specific cell structures in differential staining, e.g. acetic orcein binds to DNA and stains chromosomes dark red
Describe differences in how the image is formed between TEMs, SEMs and LSCMs
- TEM: electrons pass straight through specimen (2D black and white image);
- SEM: electrons bounce off specimen surface and focused (3D black and white image);
- LSCM: laser scans specimen point by point and stacks layers of the image at different depths (3D image)