methods of studying cells Flashcards

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1
Q

what is the first step before studying individual organelles

A

tissue is cut up

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2
Q

what is tissue kept in after being cut up + why

A

cold, buffered, isotonic solution
cold - so any digestive enzymes don’t break up cells
buffered - so ph wont change
isotonic - WP same in + out of cells - otherwise cells would burst from osmotic shock

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3
Q

how is tissue then further broken down

A

in a homogeniser

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4
Q

what is the name of teh machine the prepared, blended tissue is spun in

A

ultracentrifuge

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5
Q

what is the first spin in the centrifuge

A

low speed for 10 minutes

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6
Q

what is the role of the homogeniser

A

to blend everything evenly

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7
Q

what is the spun tissue called

A

supernatant 1,2,3

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8
Q

what is the result of the first, low speed spin

A

nucleus is heaviest
will sink to bottom
removed from supernatant 1

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9
Q

what is the part that sinks in after being spun called

A

sediment

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10
Q

what is the second spin

A

medium speed

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11
Q

what is the sediment in supernatant 2

A

chloroplasts + mitochondria

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12
Q

why is the third and final spin

A

high speed

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13
Q

what is found in supernatant 3

A

ribosomes

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14
Q

what is separating organelles by spinning them called

A

cell fractionation

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15
Q

what are the advantages of a compound light microscope

A

cheap
light and mobile
able to view living organisms
sows colour

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16
Q

what makes compound light microscopes identifiable

A

2 lenses

17
Q

disadvantages to a compound light microscope

A

low magnification (x2000 max)

18
Q

what is identifiable about transmission electron microscopes

A

electron gun
4 lenses each with a different purpose
fluorescent screen

19
Q

advantages of transmission electron microscopes

A

much higher magnification
higher resolution

20
Q

disadvantages of a transmission electron microscope

A

expensive
large
non-living specimens only
no colour
2D images only
difficult to create slides
may produce artefacts

21
Q

what is the magnification of transmission electron microscopes

A

20,000-30,000 magnification

22
Q

what do scanning electron microscope
images do

A

takes images from different angles
electrons reflect off
3D image is created off of these images

23
Q

what is the magnification of optical light microscopes

A

1500-2000

24
Q

what is the magnification of transmission electron microscopes

A

up to 50,000,000

25
Q

what is the magnification of scanning electron microscope

A

up to 1,000,000

26
Q

what is the limitations of scanning electron microscopes

A

requires a vacuum
only dead specimens
may produce artifacts

27
Q

what are artefacts

A

features that appear in the image that aren’t part of the specimen
often come in the preparation process
there was a time where scientists could differentiae between atrifacts and organelles

28
Q

formula for magnification

A

IAM magnification =size of image/actual size of specimen