Module 2- Microscopy Flashcards

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1
Q

what is resolution?

A

ability to see more detail + see individual objects as separate entities

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2
Q

what must be included in a biological drawing?

A

-title
-no shading/crosshatching
-scale
-magnification
-smooth continuous lines
-labels cannot have arrow heads

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3
Q

what is differential staining?

A

used to distinguish between two types of organism/organelles of single organism within a tissue sample

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4
Q

formula for magnification?

A

mag=image size/actual size

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5
Q

what is magnification?

A

how many times larger an image is compared to its actual size

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6
Q

what does the objective lens of a compound light microscope do?

A

produces magnified image which is magnified again by eyepiece lens

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7
Q

do transmission electron microscopes (TEM) produce 3D or 2D images?

A

2D

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8
Q

do scanning electron microscopes (SEM) produce 3D or 2D images?

A

3D

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9
Q

do laser scanning confocal
microscopes produce 3D or 2D images?

A

2D and 3D

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10
Q

image colour of laser scanning confocal
microscope?

A

coloured

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11
Q

image colour of SEM?

A

black and white

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12
Q

image colour of TEM?

A

black and white

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13
Q

which microscopes can look at live specimens?

A

light and laser scanning confocal

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14
Q

which microscope has the best resolution and magnification?

A

SEM———–electron microscopes have around the same magnifications (500 000x)

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15
Q

disadvantages of light microscope?

A

-low resolution
-poor magnification

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16
Q

advantages of light microscope?

A

-can be used on live specimens
-vacuum not needed
-small + portable
-not expensive
-natural colour observed

17
Q

disadvantages of electron microscopes?

A

-black+white images produced
-vacuum required
-cannot use live specimens
-expensive

18
Q

advantages of electron microscope?

A

-high resolving power
-high magnification

19
Q

what is an artefact?

A

visible structural detail caused by processing the specimen

20
Q

which microscopes can artefacts appear in?

A

electron and light

21
Q

how are artefacts caused in light microscopy?

A

bubbles that get trapped under the coverslip when slide is prepared

22
Q

how are artefacts caused in electron microscopy?

A

changes in cell ultrastructure during process of samples

23
Q

what is a counterstain?

A

application of a second stain with a contrasting colour to sample for microscopy

24
Q

how to use an eyepiece graticule?

A

-place the stage micrometer on the stage
-line up scales of micrometer + the eyepiece graticule
-count the number of divisions on the eyepiece graticule equivalent to each division on the stage micrometre
-calculate length of one division of the eyepiece graticule