● . If the culture from which you are preparing the slide is a liquid, simply flame your loop, allow it to cool, mix the culture, dip the loop into the culture, place loopful of culture on slide and spread out. If the culture from which you are preparing the slide is on a solid agar surface, add a small drop of water to a clean slide. Then, flame your loop or needle, allow it to cool, touch the loop on the culture, place loopful of culture on slide and spread out. In your laboratory notebook be sure to include the following: RESULTS: Draw all of the slides you viewed today. Include total magnification and titles below each of your drawings. 2. CONCLUSIONS: Differentiate between the prokaryotic and eukaryotic cells in your tooth scraping. 3. CONCLUSIONS: Explain why a slide must be air-dried and heat-fixed before staining. 4. CONCLUSIONS: Explain how a basic simple stain is able to stain bacteria. 5. CONCLUSIONS: Discuss the difference in preparation and quality of making a smear from a slant verses a broth.
● . If the culture from which you are preparing the slide is a liquid, simply flame your loop, allow it to cool, mix the culture, dip the loop into the culture, place loopful of culture on slide and spread out. If the culture from which you are preparing the slide is on a solid agar surface, add a small drop of water to a clean slide. Then, flame your loop or needle, allow it to cool, touch the loop on the culture, place loopful of culture on slide and spread out. In your laboratory notebook be sure to include the following: RESULTS: Draw all of the slides you viewed today. Include total magnification and titles below each of your drawings. 2. CONCLUSIONS: Differentiate between the prokaryotic and eukaryotic cells in your tooth scraping. 3. CONCLUSIONS: Explain why a slide must be air-dried and heat-fixed before staining. 4. CONCLUSIONS: Explain how a basic simple stain is able to stain bacteria. 5. CONCLUSIONS: Discuss the difference in preparation and quality of making a smear from a slant verses a broth.
Biomedical Instrumentation Systems
1st Edition
ISBN:9781133478294
Author:Chatterjee
Publisher:Chatterjee
Chapter19: Biomedical Laboratory Instrumentation
Section: Chapter Questions
Problem 4Q
Related questions
Question
Can you help me answer these questions (2. 3, 4, & 5?
Transcribed Image Text:. If the culture from which you are preparing the slide is a liquid, simply flame your loop, allow it to
cool, mix the culture, dip the loop into the culture, place loopful of culture on slide and spread out.
If the culture from which you are preparing the slide is on a solid agar surface, add a small drop of
water to a clean slide. Then, flame your loop or needle, allow it to cool, touch the loop on the
culture, place loopful of culture on slide and spread out.
In your laboratory notebook be sure to include the following:
RESULTS: Draw all of the slides you viewed today. Include total magnification and titles below each of
your drawings.
2.
CONCLUSIONS: Differentiate between the prokaryotic and eukaryotic cells in your tooth scraping.
3. CONCLUSIONS: Explain why a slide must be air-dried and heat-fixed before staining.
4. CONCLUSIONS: Explain how a basic simple stain is able to stain bacteria.
5. CONCLUSIONS: Discuss the difference in preparation and quality of making a smear from a slant verses a
broth.
Expert Solution
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Introduction:- Cells are the basic structural and functional unit of life. Cells are capable of independent living because of the presence of different structures like - cell membrane, that provides protection to the cell and maintains the integrity of internal environment. Living organisms can be categorised into two categories based on the number of cells present in their body - unicellular and multicellular. Unicellular organisms are made up of only single cell while the multicellular organisms consists of more than a single cell.
Dear student, i have answered the first question ( number 2) as per the Bartleby Q & A guidelines. Please post the other questions separately to get them answered.
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