mitosis and microscopes Flashcards

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1
Q

what are the two different types of microscopes

A

optical
electron

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2
Q

what is the resolution of the optical microscope

A

low

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3
Q

what is the magnification og the optical mmicroscope

A

low

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4
Q

what can thee conditions the sample be in an optical microscope

A

live

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5
Q

what is magnification?

A

how many times larger an image is compared to the OBJECT

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6
Q

what is resolution

A

the minimum distance between two points for them to appear as separate items

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7
Q

what is the equation for magnification

A

image/actual

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8
Q

what are the two types of electron microscopes

A

transmission electron
scanning electron

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9
Q

how are electrons usedd to create an image in microscopes

A

beam of electrons are condensed to create an image

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10
Q

why does an electron microscope have a high resolving power

A

electrons have a shorter wavelength

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11
Q

what is the magnification like in electron microscopes

A

high

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12
Q

what conditions can the specimen be observed under in an electron microscope

A

not living
under a vaccum

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13
Q

what does a transmission electron microscope do?

A

electrons are transmitted through specimen

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14
Q

what form is the imagee produced in TEM

A

2D

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15
Q

what conditions does the specimen need to be in TEM

A

very thin
under vaccum

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16
Q

what are the limitations of TEM

A

can contain artefacts
sample needs to be thin
vaccum so no live species

16
Q

what colour is the images from a TEM

A

black and white

17
Q

how does a scanning electron microscope work

A

electrons are beamed on the surface and is sscattered along

18
Q

what form is thee image in SEM

A

3D

19
Q

what colour is the image inn SEM

A

red

20
Q

what is the resolving power like for SEM

A

higher but lower resolving power than TEM

21
Q

what is the order of units

A

km
m
mm
micrometre
nanometre

22
Q

what is the trend for the units

A

times by 1000

23
Q

why do we use cell fractionation

A

to separate individual organelles

24
Q

what should the cell be kept in a cold colution

A

to reduce enzyme activity

25
Q

why is thee cell in a isotonic solution

A

so the water potential as the organelle
to prevent them from bursting/shrivelling

26
Q

why is the cell in a buffered solution

A

to maintain the pH so there is no damage to no organelles

27
Q

what is homganisation

A

to blend up

28
Q

why is the cell haemoginised in their cold,isotonic and buffered solution?

A

so that they are broken to release organelles

29
Q

what happens when the homogenate is created

A

it is filtered to remove LARGE cell debris

30
Q

why do we use ultracentrifugation

A

to isolate different organelles

31
Q

what happens when we spin the centrifuge at the lowest speed

A

the densest organelle is released

32
Q

what does the densest organelle form

A

pellet

33
Q

what is the supernatant

A

the mixture of organelles

34
Q

what is the order of the organelles released
when the speeed increases

A

nuclei
chloroplasts
mitochondria
lysosomes
ER
ribosomes

35
Q

how would write out the process to get chloroplast during ultracentrifugation

A

spin the supernatant and it will be in the 2nd pellet