Microscope Flashcards

(22 cards)

1
Q

What is the equation for magnification?

A

Size of image/ Actual size of image

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2
Q

Explain how to measure thee nucleus of the cells when observing the cells through a light microscope

A
  • use eyepiece graticule
  • calibrate graticule, using stage micrometer / detail of calibration / calculate the length of one epu
  • measure the diameter of the nucleus in, epu / graticule units
  • take repeat measurements and calculate a mean diameter (in epu)
  • use calibrated epu to calculate diameter (of nucleus) (in μm) / described
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3
Q

How to calibrate stage micrometer?

A
  • Place stage micrometer on stage.
  • Line up the scales of the graticule and micrometer.
  • Count the number of divisions on the eyepiece graticule equivilent to each division on the micrometer.
  • Calcutale the length of one division on the eyepiece graticule.
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4
Q

How does a scanning electron microscope (SEM) work?

A
  • it directs an electron beam onto a specimen surface.
  • The reflected electrons are amplified to produce an image.
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5
Q

How does a light microscope work?

A

light passes through lenses to produce an enlarged image of a specimen

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6
Q

How does a transmission electron microscope (TEM) work?

A
  • It transmits a beam of electrons through the specimen.
  • More dense structures absorb more electrons so they are darker.
  • Focuses image onto a fluorescent screen.
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7
Q

Magnifiction and resolution of a light microscope

A

x2000 and 200nm

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8
Q

Magnifiction and resolution of a TEM

A

x500 000 and 0.5nm

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9
Q

Magnifiction and resolution of a SEM

A

x500 000 and 3-10nm

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10
Q

How is a temporary slide prepared for a light microscope?

A
  • A thin sample of tissue is obtained.
  • Stain tissue on slide to make structures visible.
  • Add cover slip, avoiding air bubbles.
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11
Q

Image appearance of SEM

A

3D

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12
Q

Image appearance of TEM

A

2D

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13
Q

What is the function of a stage micrometer?

A

To calibrate the eyepiece graticule so it can measure structures

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14
Q

Why do samples need to me stained for a light microscope?

A

Its creates clear contrast between heavily and lightly stained areas to distiguish structures.

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15
Q

Magnification

A

the factor by which the image is larger than the specimen

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16
Q

Resolution

A

the smallest distance by which two objects can be separated and still be distinguished

17
Q

How should the field veiw in microscopy be recorded?

A

With a sharp pencil, no sketchy lines. With a scale and annotations.

18
Q

How does Laser sccanning confocal microscope work?

A
  • Laser scanning confocal microscopes work by using spot illumination (a laser) across a specimen causing fluorescence from the components labelled with a dye.
  • The emitted light is filtered through a pinhole aperture, only light radiated from very close to the focal plane is detected.
  • With a sharp pencil, no sketchy lines. With a scale and annotations.
19
Q

State the measurement conversions needed for magnification calculations.

A

1000 nanometres (nm) = 1 micrometre (um)
1000 micrometres (um) = 1 millimetre (mm)
1000 millimetres (m) = 1 metre (m)

20
Q

What is an artefact?

A
  • An artefact is a visible structural detail caused by processing the specimen and not a feature of the specimen
  • e.g. the bubbles that get trapped under the cover slip as you prepare a slide for light microscopy.
21
Q

Magnifiction and resolution of a laser scanning confocal microscope

A

54x to 17,280x and 200nm

22
Q

Image appearance of laser scanning confocal microscope