mitosis and microscopes Flashcards

(36 cards)

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

19
Q

what colour is the image inn SEM

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
what should the cell be kept in a cold colution
to reduce enzyme activity
25
why is thee cell in a isotonic solution
so the water potential as the organelle to prevent them from bursting/shrivelling
26
why is the cell in a buffered solution
to maintain the pH so there is no damage to no organelles
27
what is homganisation
to blend up
28
why is the cell haemoginised in their cold,isotonic and buffered solution?
so that they are broken to release organelles
29
what happens when the homogenate is created
it is filtered to remove LARGE cell debris
30
why do we use ultracentrifugation
to isolate different organelles
31
what happens when we spin the centrifuge at the lowest speed
the densest organelle is released
32
what does the densest organelle form
pellet
33
what is the supernatant
the mixture of organelles
34
what is the order of the organelles released when the speeed increases
nuclei chloroplasts mitochondria lysosomes ER ribosomes
35
how would write out the process to get chloroplast during ultracentrifugation
spin the supernatant and it will be in the 2nd pellet