2.1.1- cell structure Flashcards
What is the magnification and resolution of a light microscope?
magnification x1500-x2000
resolution 200nm
what is the magnification and resolution of a TEM (transmission electron microscope)
magnification x500,000
resolution 0.5nm (highest)
what is the magnification and resolution of a SEM (scanning electron microscope)
magnification x500,000
resolution 3-10nm
what are the pros and cons of a light microscope?
pros: live samples, cheaper, less expertise, colour
cons: lower resolution, lower magnification
what are the pros and cons of a TEM?
pros: highest resolution, viewing ultrastructures
cons: black and white, dead samples, expensive, 2d
what are the pros and cons of SEM?
pros: 3D images, can view surfaces
cons: black and white, dead samples, expensive, specimens must be coated in metal.
what does an eyepiece graticule do?
is calibrated to measure specimens
what does a stage micrometer do?
calibrates the eyepiece graticule at different magnifications
what is the equation for the calculation of one EPG division?
size of one stage micrometer division / number of EPG divisions covered
explain four different slide preparation techniques
dry mount: solid specimens viewed whole or sectioned. sample placed on slide and cover slip on top e.g. pollen
wet mount: specimens suspended in liquid, cover slip placed on at an angle to avoid air bubbles, e.g. aquatic samples
squash slide: wet mount prepared, lend is gently pressed to squash cells e.g. root tips
smear slides: edge of slide is used to smear sample creating a thin layer e.g. blood smear
what is positive staining?
positive stains are attracted to negative parts of a cell, including the cell components. these pick up the stain and stand out. examples include methylene blue and crystal violet.
what is negative staining?
negative stains are repelled by negative parts of the cell, so stay outside of cell components. this makes cells stand out against a stained background.
what is differential staining?
staining with multiple dyes to differentiate between different types of structures in a specimen. For example the gram-stain technique or the acid fast technique.
what is the gram-stain technique?
used to differentiate between gram positive and gram negative bacteria. crystal violet dye is added, iodine fixes the stain, slide washed with alcohol. gram positive bacteria retain the dye so appear blue/violet. a counter stain is added to highlight the gram negative bacteria, such as red safranin
what is the acid-fast technique?
used to distinguish between mycobacterium and other bacterium. Carbolfuchsin is added, cells are washed with an acid/alcohol solution. mycobacterium not affected by wash and retain the stain and show up as blue. second stain is added to highlight other bacteria, such a methylene blue.
how do you convert from millimetres to micrometres, for example 7 millimetres to micrometers
multiply by 1000. 7mm is 7000 micrometers
define magnification
how many times greater the image size is compared to the actual size
define resolution
the ability to distinguish between two separate points.