Biology 2:cells - cell fractioning and magnification Flashcards

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1
Q

whats the equation for actual size

A

image size = actual size x magnification

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2
Q

how do you work out actual size ditrectly

A

use a stage micrometer and a eyepiece graticule(rulers)
work out how many mm 1 divisions using stage micrometer
use it directly to measure cell

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3
Q

what’s the advantages of a scanning electromicroscope

A

3d surface image
high resolution and magnification

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4
Q

disadvantages of SEM and TEM(6 THINGS)

A

no living tissues
no stains (artificial colour can be added)
high voltage(expensive/dangerous)
vacum(so air is not ionised) - difficult to maintain
expensive

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5
Q

whats the advantages of Transmission microscopes

A

see inside organelles
high resolution and magnification

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6
Q

what is cell fractioning

A

getting organelles out of cells

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7
Q

name the 3 things that happen in cell fractioning

A

homogenize cells (break them apart)
differential centrifugation
results falling to the bottom of the tube (PELLet)

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8
Q

during homogenization what does the solution need to be

A

cold
same water potential as tissue
buffer

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9
Q

why does the solution need to be cold

A

to slow doen the enzymes released which could damage the organells

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10
Q

why does the solution need to have the same water potential as the tissue

A

stops organelles bursting or shrinking due to osmosis

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11
Q

why does the solution need to be a buffer

A

so ph doesn’t denature the proteins or affect the structure

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12
Q

what happens during homegenization

A

tissue is cut up and ground up in a homogenizer to break open the cells
result is called the homegenate

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13
Q

what happens in centrifugation

A

homegenate is put in centrifuge and spun

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