2.1.2: Cell Structure Flashcards
What are stains?
Coloured chemicals that bind to molecules in or on the specimen, making the specimen easy to see
What is differential staining?
When stains bind to specific cell structures, staining each structure differently so the structures can be easily identified within a single preparation.
Name 4 stains and what they do
- Acetic orcein binds to DNA and stains chromosomes dark red
- Eosin stains cytoplasm
- Sudan red stains lipids
- Iodine in potassium iodide solution stains the cellulose in a plant cell walls yellow and starch blue/black (but it appears violet under the microscope)
What are artefacts?
Artefacts are visible details that aren’t part of the specimen being observed and have been made during processing
Explain steps involved in preparing permenantly fixed slides in light microscopy
- Specimens are dehydrated
- Then they are ambedded in wax to prevent distortion during slicing
- Then a special instrument is used to make very thin slices called sections
- These are then stained and mounted in a special chemical to preserve them
What is the following for light microscopes
Magnification
Resolution
Radiation used
Focused by
Type of material that can be viewed
Size
Vacumm
Specimen made visible by
Colour
Magnification= High (x1500)
Resolution= Low (200 nm)
Radiation used= Light
Focused by= Optical/glass lenses
Type of material that can be viewed= living, moving, dead and abiotic
Size= Small + portable
Vacumm= Not necessary
Specimen made visible by= Using a stain
Colour= Yes
Technique, advantages and disadvantages of light microscopy
Technique- Light passes through the specimen into the magnifying lenses of the microscope into the objective viewing lenses into the eye
Advantages
* Relatively cheap
* Easy to used
* Study living specimens
* Portable- used in field and lab
Disadvantages
* Low resolution and limited magnification
What is the following for laser scanning confocal microscopes
* Magnification
* Resolution
* Radiation used
* Type of material that can be viewed
* Vacumm
* Specimen made visible by
* Colour
- Magnification- High, x2000
- Resolution- High but varies about 800nm
- Radiation used- Light (laser)
- Type of material that can be viewed- Living, used in medical research, components in cells
- Vacuum- Not necessary
- Specimen made visible by- Dyed with flourescent dye
- Colour- Yes
Technique, advantages and disadvantages of laser scanning confocal microscope
Techniques- Uses a laser beam to scan an object pixel by pixel, creating a 3D image of the reflected photons. 2D imaged of higher resolution can also be produced
Advantages-
* Non-invasive
* allows for observation of 3D images
Disadvantages
* Expensive
* Time-consuming
* Only see flourecent object
* Flourescence can cause aretefacts
* Requires a compromise between resolution, scan time and photodestruction of the specimen
What is the following for scanning electron microscopes
* Magnification
* Resolution
* Radiation used
* Type of material that can be viewed
* Vacumm
* Specimen made visible by
* Colour
- Magnification- High, not as good at TEM, x200 000 to x1 000 000
- Resolution- 3-20nm
- Radiation used- Electron beam
- Type of material that can be viewed- Surface of cells and organisms
- Vacumm- Yes
- Specimen made visible by- Stained with heavy metals (specifically gold)
- Colour- No
Technique, advantages and disadvantages of scanning electron microscope
Technique- Beam of electrons is sent across surface of specimen and electrons that are reflected from the surface on the specimen are detected
Advantages-
* Produce 3D images
* High magnification and resolution
Disadvantages-
* Only non-living specimens
* Large and expensive
* Need skill and training to use
* Specimens can be damaged and aretfacts can be formed
What is the following for transmission electron microscopes
* Magnification
* Resolution
* Radiation used
* Type of material that can be viewed
* Vacumm
* Specimen made visible by
* Colour
- Magnification- highest, x1 000 000
- Resolution- 0.2nm
- Radiation used- Electrons
- Type of material that can be viewed- Ultrastructure, dead specimens, thin specimens
- Vacumm- Yes
- Specimen made visible by- Stained with metal salts
- Colour- No
Technique, advantages and disadvantages of transmission electron microscope
Technique- Beam of electrons is transmitted through a specimen and focused to produce an image
Advantages- High magnification and resolution
Disadvantages
* Only dead specimens
* Large and expensive
* Need skill and training to use
* Artefacts are likely
Structure of a nucleus
Surrounded by a double membrane nuclear envelope with nuclear pores.
Contains chromosomes, consisting of protein-bound, linear DNA, and one or more nucleolus.
Contains chromatin (the genetic material)
Function of a nucleus
- The nuclear envelope sperates contents of the nucleus from rest of cell
- The pores enables larger substances to leave nucleus or enter the nucleus
- Chromosomes contain organism’s genes
- DNA replication and transcription occur in the nucleus.
Structure of the nucleolus
Spherical structure found in the cell’s nucleus and does not have a membrane around it
Function of the nucleolus
- site of ribosome production, produces and assembles ribosomes which then carry out protein synthesis
- site of rNA production
Struncture of a chloroplast
- Surrounded by a double membrane.
- Contains thylakoids, which are folded inner membrane containing chlorophyll pigments.
- Thylakoids stack to form structures called grana
- Grana are joined together by lamellae (thin and flat thylakoid membranes)
- Contains a fluid centre, the stroma.