3.1 Investigating the Structure of Cells Flashcards

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1
Q

What are microscopes?

A

Instruments that magnify the image of an object.

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2
Q

How do you calculate magnification?

A

size of image ÷ size of object

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3
Q

How do you calculate size of object?

A

size of image ÷ magnification

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4
Q

What is the resolution/resolving power of a microscope?

A

The minimum distance apart that two objects can be in order for them to appear as separate items.

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5
Q

What is the relationship between resolution and clarity?

A

Great resolution gives greater clarity.

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6
Q

What is cell fractionation?

A

The process where cells are broken up and the different organelles they contain are separated out.

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7
Q

What is the cell tissue placed in before cell fractionation?

A

A cold, isotonic, buffered solution.

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8
Q

Why is the solution cold?

A

To reduce enzyme activity that might break down the organelles.

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9
Q

Why is the solution isotonic?

A

To prevent organelles bursting or shrinking as a result of osmotic gain or loss of water.

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10
Q

What is an isotonic solution?

A

A solution that has the same water potential as the original tissue.

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11
Q

Why is the solution buffered?

A

To maintain a constant pH.

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12
Q

What are the two stages of cell fractionation?

A

Homogenation
&
Ultracentrifugation

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13
Q

What is homogenation?

A

When cells are broken up by a homogeniser, releasing the organelles from the cell. The resultant fluid is then filtered to remove complete cells and debris.

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14
Q

What is the name of the resultant fluid from homogenation?

A

Homogenate

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15
Q

What is ultracentrifugation?

A

The process whereby the fragments in the filtered homogenate are separated in an ultracentrifuge.

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16
Q

How does an ultracentrifuge work?

A

It spins tubes of homogenate at a very high speed, creating a centrifugal force.