Cell structure and microscopes Flashcards

1
Q

how does a TEM work

A

stained by metal salts
beam of electrons passing through a specimen
darker the picture the more dense structure

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2
Q

What kind of images can you see from a TEM

A

2D black and white
organelles

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3
Q

how does an SEM work

A

beams of electrons are knocked off the cell surface

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4
Q

what image do you see from an SEM

A

3D images
black and white
surface

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5
Q

why do we stain cells

A

to distinguish between cells/organelles and recognise different cells/organelles
improving contrast
to see them more clearly

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6
Q

resolution and magnification of a light microscope

A

200x
200nm

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7
Q

magnification and resolution of a TEM

A

500,000
0.5nm

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8
Q

magnification and resolution of an SEM

A

100,00 x
10nm

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9
Q

how do you use an eyepiece graticule and stage micrometer to view a specimen

A

calibrate eye piece graticule by making the divisions align

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10
Q

Outline the functions of the cytoskeleton within a cell (3)

A

Cell support / stability / scaffold / maintain shape;

Movement of flagella / cilia / undulipodia;

Cytokinesis / change shape of cell / endo / exocytosis;

Holds organelles in place;

Moves vesicles;

Moves chromosomes / mRNA;

Forms spindle / centrioles

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11
Q

glucose + glucose =

A

maltose

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12
Q

what is the purpose of gram staining

A

To differentiate between gram positive and gram negative bacteria

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13
Q

What’s the stain and colour for gram positive bacteria

A

iodine/ crystal violet –> purple/blue

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14
Q

Whats the stain for gram negative bacteria

A

acetic orcein –> DNA red/pink
eosin –>cytoplasm /pink

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15
Q

Why do specimens have to be thin in microspcopy

A

to allow light to pass through

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16
Q

What are the advantages of light microscopes

A

Cheap
Portable
Easy to use - no training
living organisms

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17
Q

What are the disadvantages of light microscopes

A

low magnification and resolution

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18
Q

What type of staining is needed for electron microscopes

A

Metallic staining - lead

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19
Q

What can you see with a laser scanning confocal microscope

A

Depth of a cell

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20
Q

Evaluate the use of laser scanning confocal microscopes

A

Disadvantages - Lower mag an res then electron
Advantages - living cells , depth

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21
Q

Evaluate the use of electron microscopes

A

Disadvantages - Expensive ,training , non living organisms
Advantages - high mag and res

22
Q

What’s the difference between the images seen in TEM and SEM

A

SEM can have added colour while TEM cant
TEM has a greater mag and res

23
Q

What do samples have to be in an electron microscope before theyre viewed

A

dehydration

24
Q

Whats the purpose of differential staining

A

Identify different cellular components and cell types

25
How are acid-fast staining techniques done
Cells are dyed and washed with acid
26
What does mycobacterium stain via acid-fast technique
Bright red
27
What stain and colour are bacteria
Methylene blue --> stain bacteria blue
28
What's the definition of magnification
Number of times larger the image is in comparison to the object
29
Define resolution
ability to distinguish between the 2 smallest points
30
How do you prepare a dry mount
thin specimen with a cover slip on top
31
How do you prepare a wet mount
place water on a slip then cover with a specimen Put the cover slip on at an angle to prevent nay air bubbles place a stain next to it and a paper towel on the other end to soak the stain in
32
What's the size of the divisions on a stage micrometre
10 um 0.01 nm
33
What's the structure and function of the nuclear envelope
double membrane to protect the cytoplasm from damage
34
What's the function of the nucleolus
site of ribosome production --> stained dark
35
What's the function of the nuclear pore
allow molecules to move in and out
36
What's the structure and function of the RER
flattened membrane bound sacs (cisternae-> synthesis occurs) covered with ribosomes transport of proteins Continuous folds with the nuclear membrane
37
What's the structure and function of the SER
fluid filled cavities no ribosomes lipid and hormone production
38
What's the structure and function of the gogi apparatus
Modifies and packages proteins into vesicles flattened membrane sacs and has secretory vesicles
39
What's the function of the ribosomes
Site of protein synthesis
40
What's the structure and function of the mitochondria
Site of ATP production double membrane - inner (cristae) surrounded by the matrix
41
What's the structure and function of the lysosomes
Spherical sacs surrounded by a membrane contains digestive enzymes - hydrolyse components and break them down
42
What's the structure and function of the chloroplast
Site of photosynthesis 2 separate membranes filled by a fluid space (stroma) flattened sacs (thykloids - that contain chloroplasts) inside chloroplasts there are granum which are joined by lamellae
43
What's the structure and function of the centrioles
Take part in mitosis to form spindle fibres Made from microtubules
44
What's the structure and function of the cell wall
Provides tensile strength insoluble maintains strength
45
What's the structure and function of the flagella
Microtubules that contract to make it move
46
What's the structure and function of the cilia
Made from protein microtubules that help cilia to move
47
How are proteins secreted
1. mRNA is made in the nucleus which leaves through the nuclear pore 2. moves to the ribosomes - where protein synthesis occurs 3. gets pinched off into a vesicle and fuses with the Golgi apparatus 4.protein becomes packaged and modified 5. vesicle travels to the plasma membrane and fuses with it 6. released by exocytosis - requires ATP
48
What are the components of the cytoskeleton and their functions
Microfilaments - change the cell shape Microtubules - move chromosomes and organelles Intermediate filaments - whole cell support
49
Compare the structure of prokaryotes vs eukaryotes
Ribosomes - 80 vs 70 Nucleus vs no nucleus Membrane bound organelles vs no membrane organelles Larger vs smaller Circular DNA vs Liner DNA Flagella in 9+2 formation vs Flagella in a helix structure
50
Whats the formula to calculate magnification
I = AM