MICRO Aseptic Technique answer sheet (1)
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Diamond Simmons
BIO 2104
March 11, 2024
Aseptic Technique Answer sheet
Pre-Laboratory Questions
1.
Is sterilization the same as disinfection? Explain your answer.
-
No, they are not the same. Sterilization is the killing of all microbes and disinfecting is the reducing and or eliminating harmful microbes from surfaces. 2.
Why is aseptic technique important?
-
This technique protects patients from bacterial and viral infections as well as protection from microbes that could be harmful. This technique keeps the equipment used during surgical procedures clean so that no contamination occurs. 3.
What are signs of microbial growth in a liquid medium, such as broth? On a solid medium, such as nutrient agar?
-
In a liquid medium cloudiness, gas bubbles, sediment at the top or bottom of the tube, and/ or color changes are signs of microbial growth. -
In a solid medium, you would see texture changes, change in color and/or transparency.
Observations Take a picture and insert it in the appropriate section below. For best results, avoid the use of flash. Do not remove the lid of the Petri dish or tube. Tilt the plates or tubes at slight angle: ©2016 Carolina Biological Supply Company
2
ACTIVITY 2: Aseptic Transfer from Broth Culture to Broth
Activity 2, Broth to Broth Transfer, 48 hours incubation Activity 2, Broth to Broth Transfer, 72 hours incubation
©2016 Carolina Biological Supply Company
3
ACTIVITY 3: Aseptic Transfer from Broth Culture to Slant
Activity 3, Broth to Slant, 48 hours incubation
Activity 3, Broth to Slant, 72 hours incubation
©2016 Carolina Biological Supply Company
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Related Questions
plz answer all the questions plz and also state the aim for this lab .. thank u
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LABORATORY REPORT: Aseptic Technique & Inoculation of Bacteria
Guide Questions.
1. Why is direct flaming preferred when disinfecting loops and needles?
2. Why is it important to flame the entirety of the loop and not just the tip? What consequences can be seen when this process is not done correctly?
3. What is the difference between quadrant streak method A from method B?
4. Why do we use a pencil instead of a pen when labelling culture tubes or plates? Are there other alternatives in labelling?
5. Why is an inoculating needle used in Subculturing Techniques? Can a loop be used instead?
NOTE: Please try to answer all of the question asked, i promised to give you a good ratings
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LAB QUESTIONS – ASSESSMENT AND CRITICAL
THINKING
1. When is a simple negative stain used?
2. Why do microorganisms remain unstained in the simple
negative staining procedure?
3. What information can be obtained from a simple positive
staining procedure?
4. What is the difference between a simple and differential
stain?
5. What is the reagent and purpose for each of the following
gram stain steps?
a. Primary stain
b. Mordant
c. Decolorizer
d. Counterstain
6. Which step is the most crucial or most likely to cause poor
results in the Gram stain? Why?
7. What part of the bacterial cell is most involved with Gram
staining, and why?
8. What cell wall component is responsible for the acid-fast
property of mycobacteria?
9. Is a gram stain an adequate substitute for an acid-fast stain?
Why or why not?
10. Which area on a streak plate will contain the greatest
amount of growth? The least amount of growth? Explain
your answers.
11. What is a colony (as viewed on an agar plate)? How can a
pure…
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Question 24 of 190
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Question is based on the following passage.
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Cancer is one of the leading causes of death in our society. Cancer is a disease in which a
cell in the body loses its sensitivity to factors which regulate cell growth and division. The
cell begins to multiply without restriction, creating a growing mass called a tumor, which
interferes with the structure and functioning of the organ in which it is located.
Frequently, cancer cells become metastatic, meaning that they travel, settling in a number of
places and giving rise to secondary tumors. Much of medical research is devoted to finding
ways of preventing, controlling, and curing cancer.
When would it be correct to reject any proposed cure for cancer?
S
O A. if it was not able to alter the ability of cancer cells to metastasize
O B. if it was based on surgery,…
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Give the uses/functions and images of each apparatuses.
Basic Laboratory Equipment
Uses/Functions
Picture
1. Microscope
2. Colony Counter
3. Autoclave
4. Microbiology incubator
5. Drying oven
6. Refrigerator (microbiology)
7. Bunsen burner/alcohol lamp
8. Candle jar
9. Anaerobic jar
10. Microhood or Bacteriologic hood/Safety hood/Safety cabinet
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Please answer the questions in the grey colored box provided in the image.
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Separation of Amino Acids by Thin Layer Chromatography Lab Questions
4. Why is it necessary to run TLC in a closed container and have the chamber saturated with solventvapor?
5. Why must the spot be applied to the TLC plate above the level of development solvent?
6. What will be the result of adding too much sample to the TLC plate?
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ANSWERS TO QUESTIONS ON
LABORATORY ASSAY NO.2
1. Why is it necessary to calibrate a Pasteur pipette?
2. Cite some possible sources of errors in the calibration of Pasteur Pipette.
3. Cite other procedural techniques that can be used for the calibration of Pasteur Pipette.
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Question 53 Which of the following risk factors would prompt a nurse to advocate for a spirometry test for a COPD diagnosis?
Question 53 options:
Frequent respiratory tract infections
History of smoking and over the age of 40
Daily puffer use
Persistent cough for the past 2 weeks
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Hand written plz asap.... Fast plz plz asap plz i need urgent
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Hand written plz otherwise downvote...fast plzzzzzzzzzzzzz
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I need help with microbiology/2010
1. Describe where the following items should be discarded:
a) gloves
b) petri dishes
c) test tubes
d) microscope slides
2. Describe the safety procedures for the following hypothetical situations:
a. You spilled a full test tube of bacterial culture on the bench top.
b. You notice flames coming from the tubing of your Bunsen burner
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Question:-
Describe control strains used in the clinical microbiology laboratory and explain their maintenance in the laboratory. ( write BY WORD and all steps I need).
Introduction
Discussion
References
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Anaerobes question attached
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I only need question 2 please,
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1.
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Please Help
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QUESTION:
Microbes from a blood culture inoculated with blood drawn from a catheter were determined by the appearance of growth on Mannitol Salts Agar and through other tests to be Staphylococcus epidermidis. It can be concluded that:
a.
a bloodstream infection caused by S. epidermidis is occurring in the patient from whom the blood was drawn
b.
The bacteria fermented mannitol, changing the color of the growth medium from pink to yellow.
c
S. epidermidis is present in the sample as a normal flora contaminant
d.
That in order to determine if a bloodstream infection is present, these results must be compared to a blood culture of a sample drawn from a peripheral vein
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this lab was carried out the results are in the picture below plz provide a aim for this lab abd answer thw questions below
the method used is also stated
Title: Bacterial Inhibition
Aim:
Materials:
Streak plate from LAB # 3
Disks
Ethanol (dilutions of 20%, 50%, 70%, 95%)
Burner
Flame
Matches
Tape
Method:
Ethanol was used to clean the work station
A maker was used to dived each equal sections and ruler and was label with appropriate concentrations.
The plate carefully open
The disc was soak in the different concentrations of ethanol
Placed one disc per concentration for each labelled section
The plate was tape shut
The plate was returned to the incubator
The zone of inhibition was recorded after 3 days.
question 1 state a aim
question 2 in a table format plz explain the bacteria growth of e.coil and staph and state any two limation of this lab
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Give the uses/functions and images of each apparatuses.
Basic Laboratory Equipment
Uses/Functions
Picture
6. Refrigerator (microbiology)
7. Bunsen burner/alcohol lamp
8. Candle jar
9. Anaerobic jar
10. Microhood or Bacteriologic hood/Safety hood/Safety cabinet
11. Bacteriologic filters (Seitz, Chamberlain, Berkfield)
12. Petri dish
13. Culture tubes
14. Hanging drop slide
15. Durham’s tube
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Question:-
Your medical care team determines that a third patient's severe illness is caused bya helminth. Which technique or techniques described above would you use to identifythe helminth? Justify your answer.
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Practice Question Chapter 3
Another source of contamination cheesemakers really worry about are
bacteriophages. Entire batches of cheese can be ruined in a matter of days by
bacteriophages infecting lactic acid bacteria.
4. Should cheesemakers be worried about endospore growth of Gram-positive cells?
Why or why not?
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Differential staining procedures gray stain and acid-fast stain lab report.
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Give the uses/functions and images of each apparatuses
Basic Laboratory Equipment
Uses/Functions
Picture
21. Antibiotic disk
22. Antibiotic dispenser
23. Weighing balance
24. Forceps
25. Stains/Staining reagents
26. Culture media/Culture plates
27. Culture swabs
28. Gloves
29. Mask
30. Caliper ruler
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INSTRUCTIONS:
Please do not copy here in Bartleby or in Google.
QUESTIONS :
1. Aside from using the autoclave, what are other ways to kill microorganisms from glassware that can be use in the laboratory?
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SEE MORE QUESTIONS
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Related Questions
- plz answer all the questions plz and also state the aim for this lab .. thank uarrow_forwardLABORATORY REPORT: Aseptic Technique & Inoculation of Bacteria Guide Questions. 1. Why is direct flaming preferred when disinfecting loops and needles? 2. Why is it important to flame the entirety of the loop and not just the tip? What consequences can be seen when this process is not done correctly? 3. What is the difference between quadrant streak method A from method B? 4. Why do we use a pencil instead of a pen when labelling culture tubes or plates? Are there other alternatives in labelling? 5. Why is an inoculating needle used in Subculturing Techniques? Can a loop be used instead? NOTE: Please try to answer all of the question asked, i promised to give you a good ratingsarrow_forwardLAB QUESTIONS – ASSESSMENT AND CRITICAL THINKING 1. When is a simple negative stain used? 2. Why do microorganisms remain unstained in the simple negative staining procedure? 3. What information can be obtained from a simple positive staining procedure? 4. What is the difference between a simple and differential stain? 5. What is the reagent and purpose for each of the following gram stain steps? a. Primary stain b. Mordant c. Decolorizer d. Counterstain 6. Which step is the most crucial or most likely to cause poor results in the Gram stain? Why? 7. What part of the bacterial cell is most involved with Gram staining, and why? 8. What cell wall component is responsible for the acid-fast property of mycobacteria? 9. Is a gram stain an adequate substitute for an acid-fast stain? Why or why not? 10. Which area on a streak plate will contain the greatest amount of growth? The least amount of growth? Explain your answers. 11. What is a colony (as viewed on an agar plate)? How can a pure…arrow_forward
- srv/test/819 Federal Stu... Amazon ClassMarker Rosults Question 24 of 190 FINAL - Science NYS DMV - My DMV 14.udemy NYC HEALTH +HOS.... ClassMarker - Test Question is based on the following passage. LaGuardia VIP (Log... NY Cancer is one of the leading causes of death in our society. Cancer is a disease in which a cell in the body loses its sensitivity to factors which regulate cell growth and division. The cell begins to multiply without restriction, creating a growing mass called a tumor, which interferes with the structure and functioning of the organ in which it is located. Frequently, cancer cells become metastatic, meaning that they travel, settling in a number of places and giving rise to secondary tumors. Much of medical research is devoted to finding ways of preventing, controlling, and curing cancer. When would it be correct to reject any proposed cure for cancer? S O A. if it was not able to alter the ability of cancer cells to metastasize O B. if it was based on surgery,…arrow_forwardGive the uses/functions and images of each apparatuses. Basic Laboratory Equipment Uses/Functions Picture 1. Microscope 2. Colony Counter 3. Autoclave 4. Microbiology incubator 5. Drying oven 6. Refrigerator (microbiology) 7. Bunsen burner/alcohol lamp 8. Candle jar 9. Anaerobic jar 10. Microhood or Bacteriologic hood/Safety hood/Safety cabinetarrow_forwardPlease answer the questions in the grey colored box provided in the image.arrow_forward
- Separation of Amino Acids by Thin Layer Chromatography Lab Questions 4. Why is it necessary to run TLC in a closed container and have the chamber saturated with solventvapor? 5. Why must the spot be applied to the TLC plate above the level of development solvent? 6. What will be the result of adding too much sample to the TLC plate?arrow_forwardANSWERS TO QUESTIONS ON LABORATORY ASSAY NO.2 1. Why is it necessary to calibrate a Pasteur pipette? 2. Cite some possible sources of errors in the calibration of Pasteur Pipette. 3. Cite other procedural techniques that can be used for the calibration of Pasteur Pipette.arrow_forwardQuestion 53 Which of the following risk factors would prompt a nurse to advocate for a spirometry test for a COPD diagnosis? Question 53 options: Frequent respiratory tract infections History of smoking and over the age of 40 Daily puffer use Persistent cough for the past 2 weeksarrow_forward
- Hand written plz asap.... Fast plz plz asap plz i need urgentarrow_forwardHand written plz otherwise downvote...fast plzzzzzzzzzzzzzarrow_forwardI need help with microbiology/2010 1. Describe where the following items should be discarded: a) gloves b) petri dishes c) test tubes d) microscope slides 2. Describe the safety procedures for the following hypothetical situations: a. You spilled a full test tube of bacterial culture on the bench top. b. You notice flames coming from the tubing of your Bunsen burnerarrow_forward
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SEE MORE QUESTIONS
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Recommended textbooks for you
- Comprehensive Medical Assisting: Administrative a...NursingISBN:9781305964792Author:Wilburta Q. Lindh, Carol D. Tamparo, Barbara M. Dahl, Julie Morris, Cindy CorreaPublisher:Cengage LearningSurgical Tech For Surgical Tech Pos CareHealth & NutritionISBN:9781337648868Author:AssociationPublisher:Cengage
Comprehensive Medical Assisting: Administrative a...
Nursing
ISBN:9781305964792
Author:Wilburta Q. Lindh, Carol D. Tamparo, Barbara M. Dahl, Julie Morris, Cindy Correa
Publisher:Cengage Learning
Surgical Tech For Surgical Tech Pos Care
Health & Nutrition
ISBN:9781337648868
Author:Association
Publisher:Cengage