Lab based research methods Flashcards

1
Q

What are the types of microscope?

A

1.Stereo :
- reflected light
- can see 3D
2. Compound:
- transmitted light
- requires microscope slide and coverslip (may damage sample)
3 . Inverted:
- transmitted light from above
- objects are below the stahe
- can view samples in a petri dish

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2
Q

What is phase contrast microscopy?

A
  • allows live cells to be observed more eaily with no fixation or labelling
  • works well with thin speciments
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3
Q

What are some advantages of immunohistochemistry?

A
  • straightforward technique
  • can be applied to any tissue provided antibody is available
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4
Q

Limitations of immunohistochemistry

A
  • limited resolution
  • tissue has to be fixed - could lead to artefacts
  • need to have an antibody to the protein of interest
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5
Q

What are some advantages of phase contrast and DIC microscopy?

A
  • allows live cells to be observed more easily with no fixation or labelling
  • relatively inexpensive (compared to other types of microscopes)
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6
Q

What are some limitations of Phase contrast and DIC microscopy?

A
  • poor resolution
  • cannot identify specific proteins or structures
  • 2D images
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7
Q

What is fluorescent molecule?

A
  • one that absorbs light of a particcular wavelength and emits light of a different wavelength
  • fluorescent stains binf specific molecules:
  • DAPI and Hoeschst - bind minor groove of DNA so label nuclei
  • phalloidin stains actin
  • Fluo3 binds calcium
  • can create fluorescent drugs
  • intesity of fluorescence can be quantified
  • fluorescence decreases with increasinf concentration of antagonist
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8
Q

Advantages of fluorescence microscopy

A
  • can identify specific proteins if antibody is available
  • can measure concentrations of intracellular signalling molecules/ions e.g. calcium, chloride
  • useful in live cells
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9
Q

Limitations of florescence microscopy

A
  • prolonged light can cause fading of fluorescence
  • not sure whether the prescence of fluorophore can affect intracellular signalling or be toxic to cells
  • 2D images
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10
Q

What are confocal fluorescence /laser scanning microscopes?

A
  • uses lasers to give specific wavelengths
  • confocal microscope = able to focus on a thin layer
  • it scans accross the image and then at difffferent depths
  • builds up a 3d image
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11
Q

What are some examples of multiple fluorescent staining?

A
  • Human cancer cell
  • DNA stained blue
  • Microtubules are stained red
  • protein (INCENP) stained green
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12
Q

What is live cell imaging?

A

If a cell as been transfected with a GFP-linked protein, fluorescence imaging can occcur in live cells
GFP = green fluorescent protein

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13
Q

Examples of fluorescent indicator molecules?

A
  • Fluo3-AM
  • Fura
  • Oregon Green
  • Rhod 2
  • They fluoresce when the calcium concentration – icnreases and intensity relates to concentration of calcium
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14
Q

What is Live vs Fixed imaging?

A
  • cells can be fixed with formaldehyde and then incubated with fluorescently-labelled antibodies
  • other fluorescent chemical
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15
Q

What are advantages of confocal microscopy?

A
  • can be used for live or fixed cells
  • can detect specific proteins or ions/molecules (provided suitable fluorophore available)
  • can build 3D image
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16
Q
A
17
Q

What are some limitations of confocal microscopy?

A
  • restricted to wavelengths avaialable from lasers
  • expensive
18
Q

What is electron microscopy?

A
  • uses beams of electrons rather than light
  • electron beams have shorter wavelength than light
  • have higher resolution -1000000x magnification
  • requires a lot of sample preparation (dehydration and embedding within resin then sliced very thinly)