A2.2 Cell structure Flashcards
State the three parts of the cell theory.
- All living things are composed of cells
- The cell is the basic unit of life
- Cells come from pre-existing cells
Compare the use of the word theory in daily language and scientific language.
Daily use : a guess there is a doubt
Scientific use : a theory has been shown to be true through repeated observations and experiments. As of yet, no evidence has been collected that contradicts the idea.
Distinguish inductive from deductive reasoning.
Inductive reasoning is when you use observations to form a conclusion
Deductive reasoning is when you use knowledge to predict the result
Outline the process of inductive reasoning that led to the development of the cell theory.
Inductive reasoning
- In all the specimen that biologists have seen they have seen one or more cells, therefore all living things are made of cells
- Subcellular components can’t function whereas full cells have therefore the cell is the most basic unit of life.
- We have seen cells come from other cells but never seen spontaneous generation, therefore cells come from cells
Outline how deductive reasoning can be used to predict characteristics of a newly discovered organism.
Deductive reasoning used the cell theory to predict that slime molds were made of cells.
Given the magnification of the ocular and objective lenses, calculate the total microscope magnification.
TOTAL MAGNIFICATION = OCULAR X OBJECTIVE
Demonstrate how to focus the microscope on a sample.
Begin with the lowest magnification objective lens, use the coarse focus knob to raise the stage until the sample is in view, and then adjust the fine focus knob for precise focusing. It is important to follow proper safety procedures and handle the microscope carefully throughout the process.
Demonstrate how to make a temporary wet mount and stain a microscopic sample.
Place a sample on the slide
Using a pipette, place a drop of water on the specimen
Place the edge of the cover over the sample at an angle and carefully lower the cover slip into place.
If there is too much water, the cover slip will slide around. Place a paper towel and hold it close to the slip to absorb the water
Measure the field of view diameter of a microscope under low power.
Place a transparent metric ruler under the low power objective lens to measure the diameter of FOV on low power magnification
Calculate the field of view diameter of a microscope under medium or high power.
Use the equation
(Diameter (LP) x Magnification of LP objective )/ Magnification of HP objective
Use a formula to calculate the magnification of a micrograph or drawing.
Magnification = size of image / actual size of specimen
If given the magnification of a micrograph or drawing, use a formula to calculate the actual size of a specimen.
Estimate the number of the specimen you could fit across the FOV then divide the FOV by that number
Compare quantitative and qualitative observations.
The drawings of the cells are qualitative observations where you give cell characteristics whereas the quantitative observation is where you measure the size of specimens or FOV.
Define resolution and magnification.
Resolution : the smallest interval distinguishable by the microscope, which then corresponds to the degree of detail visible in an image created by the instrument.
Magnification : how much larger it appears in comparison to real size
Compare the functionality of light and electron microscopes.
Light microscopes
Benefits
1. Ease of use
2. Less expensive
3. Can observe dead or living cells in color
4. Cell movement can be studied
5. Quick specimen prep
6. No need for high voltage
Limitations
1. Maximum magnification of about 1500X
2. Low resolving power
Electron microscopes
Benefits
1. Magnification of 100,000 X to 300,000X
2. High resolving power
Limitations
1. Expensive
2. Requires cells to be killed
3. No movement can be seen
4. No color can be seen without stain or dye
5. High voltage required
6. Specimen prep takes a few days
Outline the process of visualizing specific proteins in cells using immunofluorescence technology.
Immunofluorescence technology is a technique that uses fluorescently stained antibodies to bind specific target proteins. so that these proteins can be tracked as it moves in a cell.