cell structures

Cards (62)

  • resolution = the minimum distance between two objects in which they can still be viewed as separate.
  • Magnification = how many times larger the image is compared to the object
  • How to prepare a dry mount ?

    Thin slice of specimen and place cover slip over top
  • How to prepare a wet mount ?

    Water is added on top of specimen before cover slip is placed on at an angle to prevent air bubbles.
  • How to prepare a squash slide ?

    A wet mount which you apply force to coverslip to squash the slide
  • When would a squash slide be used ?
    To view chromosomes in mitosis of a root tip
  • How to prepare a smear slide ?

    Place a drop of sample at one end and using the edge of slide smear sample across to create a thin, smooth even coat.
  • When would you use a smear slide ?

    To look at cells in a blood test
  • Eyepiece graticule = a scale on a glass disc which can be inserted inside a light microscope
  • How to calibrate an eyepiece graticule ?
    1. line up stage micrometer and eyepiece graticule
    2. count how many divisions on the eyepiece graticule fit into one division on stage micrometer scale
    3. calulate what 1 division on the graticule is worth
  • What is the value of one division on a micrometer ?

    10 micrometres
  • what is the purpose of staining ?

    to allow differentiation between cell components
  • differential staining = many chemical stains being used to stain different parts of as cell in different colours
  • Name 2 positive stains ?
    Crystal violet
    Methylene blue
  • Name 2 negative stains ?
    Congo red
    Nigrosin
  • Why do negative stains only stain the background ?

    The cytosol repels them so the stains cannot enter the cell.
  • Why do electron microscopes have such high resolution ?

    Beams of electrons have a short wavelength
  • What is the main advantage to electron microscopes ?

    Can see small organelles
  • What are the disadvantages to electron microscopes ?

    only in black and white
    specimen must be non-living
    Must be in a vacuum
  • Name 3 key differences between transmission and scanning electron microscopes ?

    • transmission creates 2D images, scanning creates 3D images
    • Transmission shows internal structures, scanning shows external structure
    • Transmission must have thin specimen, scanning it does not matter
  • Laser scanning confocal microscope = fluorescent microscope
  • How does a laser confocal microscope create its images ?

    The high light intensity illuminates the specimen stained with a fluorescent dye.
  • What are 3 benefits to laser confocal microscope ?

    high resolution image
    depth selectivity
    view sections of tiny structures
  • What are the 5 components of the nucleus ?

    nuclear envelope
    nucleoplasm
    nuclear pores
    chromosomes
    nucleolus
  • What is the function of the nucleus ?

    Site of ribosome synthesis
    Contains DNA for each cell
    Site of DNA replication and transcription
  • What is the function of nuclear pores ?

    Allow mRNA to pass out of nucleolus after transcription
  • What is the function of nucleolus ?

    Site of rRNA production and ribosome synthesis
  • Functions of flagella ?

    mobility
    sensory organelle for chemical stimuli
  • Functions of cilia ?
    Movement of substances
    Sensory
  • What is centrioles made from ?

    Microtubules
  • What is a centrosome ?

    A pair of centrioles
  • Function of centrioles ?

    Spindle fibre formation and organisation of chromosomes in cell division
  • cytoskeleton = network of fibres found within the cytoplasm all over a cell
  • What is the function of cytoskeleton ?

    Cell/organelle movement
    maintain shape
    provides mechanical strength
  • Describe structure of smooth Endoplasmic reticulum ?

    folded membranes
  • Describe the structure of rough Endoplasmic reticulum ?

    Folded membrane studded with ribosomes
  • What is the function of smooth E.R?

    synthesis and storage of lipids/carbohydrates
  • What is the function of rough E.R ?

    Synthesis of proteins
  • Structure of the golgi apparatus ?

    Folded membrane, with a constant shape evolution due to vesicles binding and pinching off
  • Function of Golgi ?

    Storage, modification and packaging of proteins