2.1 Cell Structure Flashcards
Describe how a light microscope works.
•Lenses focus rays of light and magnify the view of a thin slice of a specimen
•Different cellular structures absorb different amounts of wavelengths of light
•Reflected light is transmitted to the observer via the objective lens and the eyepiece
Describe how a transmission electron microscope (TEM) works.
•A high energy bean of electrons is passed through a thin slice of specimen
•The more dense of the cellular structures appear darker as they absorb more electrons
Describe how a scanning electron microscope (SEM) works.
•A beam of electrons is focused onto a specimen’s surface using electromagnetic lenses
•Electrons are then reflected off of the specimen and into a collecting device, which generates an image
Describe how a laser scanning confocal microscope works.
•A laser beam is focused onto a small area on a sample’s surface using objective lenses
•A fluorescent stain is added to the sample, which reflects the laser
•A detector then generates an image of the sample pixel by pixel.
How should field of view in microscopy be recorded?
•Draw diagram of image
•Include scale bar
•Annotate visible structures
State an equation to calculate the actual size of a structure from microscopy.
•Image size = Actual size x Magnification
Define magnification and resolution
•Magnification: the factor by which the image is larger than the actual specimen
•Resolution: the smallest separation distance at which 2 separate structures can be distinguished from one another
Why do samples need to be stained for light microscopes ?
•Coloured dyes bind to the structures
•Allows for the absorption of some wavelengths of light to produce an image with contrast.
What is differential staining ?
•Contrast between heavily and lightly stained areas, allows for distinguishing structures.
State the magnification and resolution of a optical light microscope.
•Magnification : x2000
•Resolution : 200nm
State the magnification and resolution of a TEM.
•Magnification : x500,000
•Resolution : 0.5nm
State the magnification and resolution of a SEM.
•Magnification : x500,000
•Resolution : 3-10nm
Explain how to use the eyepiece graticule and stage micrometre to measure the size of a sample’s structures.
•Place micrometre on stage to calibrate eyepiece graticule
•Line up scales on graticule and micrometre. Count how many graticule divisions are in 100µm on mictometre
•Length of 1 eyepiece division = 100µm / number of divisions
•Use calibrated values to calculate actual length of structures
Describe the structure of the nucleus.
•It is surrounded by a semipermeable double membrane called the nuclear envelope
•Nuclear pores allow substances to enter/exit
•Dense nucleolus made of RNA and proteins, assembles ribosomes.
Describe the function of the nucleus
•Contains DNA coiled around chromatin into chromasones
•Controls cellular processes: gene expression (specialisation and site of mRNA transcription), mitosis, semiconservative replication