History of Cell Bio and Microscopy Flashcards

1
Q

Process of sectioning:

A
  1. Fix tissue
  2. Remove water from cells
  3. embed them in a rigid agent (parrafin for LM, plastic for EM) for cutting into thin
  4. remove embedding and add water back in
  5. mounting agent
  6. look at sample
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2
Q

condenser focuses light on _____

objective and eyepiece focus light on ____

A

specimen

eye

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3
Q

Type of microscopy that:

  • displays differences in light intensity.
  • details down to 0.2micrometers
  • best if used w stains
  • bad resolution
  • cant see much of live specimens
A

bright field microscopy

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4
Q

Type of microscopy that:

  • displays differences in phase of light bouncing around specimen as differences in contrast (visible to eye)
  • higher contrast (can get better resolution w/o staining
  • live samples
  • need thin specimen
A

phase or interference contrast microscopy

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5
Q
  • picks up indirect light scattered off structures rather than direct light passing through
  • seeing borders and surfaces of samples; seeing tiny structures
  • can be used for live samples
  • lwo light level can make it hard to see things, but more incident light could be bad for sample
A

dark field microscopy

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6
Q

type of microscopy that:

  • marks specific structures using immunocytochemistry: with an immobilized sample:
  1. primary Ab to Ag of interest
  2. 2ndary antibody attached to fluorophore against primary Ab
  3. excite fluorophore, “see” Ag
  • identifying location of specific structures, tracking structures before and after an intervention
  • expensive, have to know what you’re looking for and make Abs, have to excite with specific wavelength with fluorophore
  • can see many diff proteins by fluorescing at different wavelengths
A

fluorescence microscopy

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7
Q
  • upside-down light microscope
  • increase speed of electrons decreases wavelength (??)
  • magnetic lenses focus beam of electrons on fluoresent screen
  • resolution up to 0.001 micrometers (1 nm)
  • can see cellular details
  • super expensive, only works for certain structures
  • putting oil between lens and slip gives higher resolution
A

electron microscopy

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8
Q
  • works by interference of light waves as a result of distortion by cellular component. Light forms series of diffraction lines and our eye interprets this additive and subtractive interference
A

light microscopy

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