Magnification: The number of times bigger the image/drawing is compared to the object/real size.
Resolution: The minimum distance needed to differentiate between 2 adjacent objects.
Micrometer: 1 x 10-6m
Nanometer: 1 x 10-9m
The material that is put under a microcsope is referred to as the object.
The apperance of the material when viewed under the microscope is called the image.
Magnification = size of image ÷ size of real object
The reolution can also be called resolving power.
The resolving power depends on the wavelength or form of radiation used in the microscope.
Increasing the magnification increases the size of the image, but dosen't always increase the resolution.
Cell Fractionation: The process where cells are borken up and the different organelles they contain are separated out.
Homogenation: The first stage of cell fractionation when cells are broken up by a homogeniser (blender) and organelles are released from the cell.
Ultracentrifugation: The second stage of cell fractionation when the fragments in filtered homogenate are separated in a centrifuge.
Before cell fractionation can begin cells must be placed in a cold, buffered solution of the same water potential as the tissue.
Cells before cell fractionation are placed in a cold solution to reduce enzyme activity that might break down organelles.
Cells before cell fractionation are placed into a buffered solution so that the pH dosen't fluctuate. Changes in pH could alter the structure of organelles or affect the functioning of enzymes.
Cells before cell fractionation are placed into a solution with the same water potental as the tisssue to prevent cells from bursting ot shrinking as a result of osmotic gain or loss of water.
After homogenation cells are filtered to remove any large pieces of debris. They then go into the centrifuge.
A centrifuge is first spun slow and the heaviest organelles are forced to the bottom where they form a thin sediment. Then the speed is increased and the next heaviest organelle will form the same process.