2.1 Cell Structure Flashcards
What was research like before and after microscopes?
Before- no knowledge of bacteria, cells, etc.
After- power to understand disease, cell division, beginnings of life, etc.
Definition of Magnification
How many times an image appears larger than the actual size of the object being magnified.
Who developed first microscope and when was the first cell observed?
Robert Hooke developed first microscope in the 17th century.
In the 19th century, an individual cell was first observed by Robert Brown.
What are cells?
Cells are basic unit of life and can only develop from existing cells.
Both plant and animal tissue is made up of cells.
Definition of Resolution
Smallest distance between 2 points that can still be seen as 2 points.
Dry Mount
-View small inanimate objects that don’t require water.
-Can be viewed whole or as thin slices.
-Eg. hair, pollen, dust.
Wet Mount
-Suspend specimens in liquid.
-Add cover slips at an angle.
-Allows small aquatic organism to be seen.
Squash Slides
-Wet mount first applied
-Pressure then applied to squash sample, so this is thin enough for light to pass through and removes excess liquid.
-Eg. mitosis in root meristem.
Smear Slides
-Edge of slide used to smear a sample creating thin, even coat.
-Cover slip added at an angle.
-Eg. Observing blood.
What is staining used for?
Used to increase contrast with different cellular components. Different cellular components take up stain to different degrees making them more or less visible.
Positively charged stains
Are attracted to negatively charged materials, staining components.
Eg. Crystal violet, methylene blue.
Negatively charged stains
Are repelled by negative cytosol (aqueous interior in cells). Dyes stay outside of cells, so cells are unstained making them more visible.
Eg. Nigrosin, Congo red.
What is differential staining?
Distinguishing between 2 types of organism that would be hard to identify. Also differentiates between different organelles of an organism within a tissue sample.
Gram positive bacteria
Has thick pepticloglycan layers so absorb surrounding materials.
Gram negative bacteria
Has thin wall so loses any stain. Then stained again with a different stain to differentiated between other types of bacteria.
What is acid-fast technique?
Distinguishes between mycobacterium and other bacteria.
Acid-Fast Technique Method
1) Lipid solvent carry’s carbolfuchsin dye to cells being studied.
2) Cells wash with dilute acid-alcohol solution. Mycobacterium are not affected and retain bright stain.
3) Other bacteria lose stain and are exposed to methylene blue stain.
Bacteria Staining Method
1) Crystal violet is applied to bacterial specimen slide.
2) Iodine is then added, fixing the dye.
3) Slide is washed with alcohol.
4)Gram positive bacteria retain crystal violet stain appearing blue.
5) Gram negative bacteria have thinner cell walls and lose the stain. They are then stained with safranin dye making them appear red.
How do electron microscopes work?
They use beams of electrons instead of light rays.
Why do electron microscopes have a higher resolution?
Electron beams have shorter wavelengths than light microscopes, which results in a higher resolution .
Millimeter to micrometer conversion
x1000 for conversion to smaller unit.
Equation for magnification
Magnification-Image size/ Actual size.
Calibration method
1) Find relationship between eye piece graticule and stage micrometer.
2) Multiply by actual size of object.
Eyepiece graticule
Ruler in the eyepiece lens.
Stage micrometer
Ruler on specimen slide.
Features of electron microscope
-x 500,000 magnification.
-Cells ultra structure is visible.
-Very expensive and hard to use.
-Specimens can be damaged by electrons.
-Complex preparation process, which can lead to artifacts.
Transmission Electron Microscope (TEM)
Beam of electrons transmitted through specimen, which is focused to produce an image.
-Similar to light microscopy.
What is the resolution of transmission electron microscopes?
0.5 nm.
What is resolution of scanning electron microscopes?
3-10 nm.
How does laser scanning con-focal microscopy work?
Single spot of focused light moves across specimen that has been marked with fluorescent dye.
Use of fluorescence in laser scanning con focal microscopy.
Fluorescence is used for absorption and re-radiation of light.
Re-radiated light in laser scanning con focal microscopy.
Re-radiated light has longer wavelength and lower energy.
Filtered through a pinhole aperture and unwanted radiation doesn’t pass through, which reduces resolution.
Application of Laser Con focal Scanning Microscopy.
-Non invasive.
- Can diagnose eye diseases
-Used in development of new drugs.