2. Cell Fractionation Flashcards

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1
Q
A
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2
Q

Give two ways homogenisation is done?

A

Using sound waves and vibrating the cellsGrinding them in a blender

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3
Q

What is the order organelles come out?

A

Nucleus
Chloroplasts
Mitochondria
Lysosomes
ER
Ribosomes

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4
Q

Why is microscopy useful in studying cells?

A

Allows us to see organelles

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5
Q

What do the techniques of fractionation and ultracentrifugation allow us to do?

A

separate organelles to study function

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6
Q

What happens during fractionation?

A

Cells broken open

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7
Q

What happens during ultracentrifugation?

A

Organelles separated

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8
Q

What tissue is commonly used? Why?

A

Liver (1) High metabolism/ lots of organelles

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9
Q

Why is a buffer solution used?

A

To maintain a constant pH

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10
Q

Why the solution is used isotonic?

A

to prevent water entering or leaving the organelles so stops them shrinking or bursting

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11
Q

Why is everything kept ice-cold?

A

To prevent enzyme activity

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12
Q

Which organelle contains enzymes that might damage the cells or its contents?

A

Lysosomes

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13
Q

Why is the sample homogenised

A

To break open cells and release organelles

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14
Q

Why is the homogenate filtered

A

To remove cell debris

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15
Q

Initially the homogenate is spun at low speed. Suggest what this might be.

A

800-1000g/ 10 mins

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16
Q

Why does a pellet separate out?

A

Some organelles are heavier and more dense

17
Q

What is the first organelle to separate out?

A

Nuclei

18
Q

Give another name for the pellet?

A

sediment

19
Q

What is the liquid called?

A

Supernatant

20
Q

The liquid is centrifuged again at a higher speed e.g. 3-4000g for 10 minutes. Suggest what will separate out now.

A

Mitochondria

21
Q

Suggest a tissue you could use to obtain a sample of chloroplasts

A

Spinach