Aseptic Technique answer sheet (1)

Questions: 1. What happens to the number of bacteria as you streak from one sector to another? 2. What happens to the colonies when the bacteria are separated well? 3. How bacteria does each colony come from? many 4. Why do you make sure that the inoculating loop is red hot? 5. What happens when the streaking is not correct? 6. When do you flame the mouth of the cultures tubes? 7. Why you should not use the inoculating loop when it is red hot?

drop down options. 1. staphlococcus aureus/ Pseudomonas aeruginosa. 2. gram negative /gram positive 3. gram negative /gram positive 4. regular soap, isopropyl alcohol, lysol, antibacterial soap, mouth wash, hydrogen peroxide 5. vinegar, ajax, bleach, lysol, windex, and isopropyl alcohol. Which bacterium was more resistant to the chemicals over-all? (Hint-which bacterium had more results of Omm and generally smaller zones of inhibition overall?). Staphylococcus aureus . This result makes sense because [Select] and disinfectants than [Select] Which chemical produced large (>20mm) zones of inhibition against both bacteria? [Select] tend to be more resistant to antiseptics Which chemicals produced no zones of inhibition against either bacteria? [Select]

I need help

Item 1.      Describe the BEST method of sterilization or treatment to reduce pathogens to safe level for each of these 5 items. 2.      Explain why this is the best method and why it is BETTER than other possible methods. (Specific treatments were mentioned in lecture for each item.)  Plastic milk containers  1. Preserving low-acid vegetables to kill Clostridium botulinum endospores.  2. Liquids contaminated with prions (list BOTH methods of sterilization discussed in lecture)  3. Skin  4. Media with heat sensitive nutrients  5.

Please answer the questions

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…

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

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

Short answer quickly

INSTRUCTIONS: Read each sentence carefully Encircle the biological techniques that are being described. 1. Itis also known as sterile technique. Aseptic technique Disinfection Answer: 2. It is described as the complete removal of microorganisms found in a specimen or sample. sterilization Disinfection Answer: 3. It is described as the elimination of pathogens that reduce the microbial contamination. sterilization Disinfection Answer: 4. This is described as the elimination of life processes in a specimen. Killing Fixation Answer: 5. Clearing is also known as Dehydration Dealcoholization Answer:

i need the answer quickly

困 Topic: laboratory Instrument Which of the following are TRUE regarding Which of the following is/are TRUE the use of laboratory instruments and regarding the use laboratory instruments equipment in regards to making of culture media? " and equipment? * Air bubbles on the surface of agar plates Hot plates can be used to sterilize the inoculating loop and needle. can be removed by fanning them with the luminous flame of the bunsen burner. If the agar surface is wet, it can be dried by A drying oven is used to sterilize nutrient agar, a solid culture medium. heating at 30-40 deg C in the drying oven before inoculation is done. The refrigerator is used to grow psychrophiles. All media taken from the refrigerator should be warmed to room temperature before use, P Type here to search 7:11 pm 30/09/2021 ヘロG) ENG 近

True / False 1. Sterilization can penetrate most soil, so there is no need to clean a surgical instrument prior to sterilization. 2. One of the greatest challenges in infection control of reprocessed medical devices is a lack of consistent understanding of what the definition of "clean" is.

INSTRUCTION: Give the principle or significance of the following practices:   1. Flaming the mouth or lid of culture tubes or plates after opening and before closing them. 2. Flaming the inoculating needle or loop before and after inoculation. 3. Holding caps, lids, or cotton plugs rather than putting them on the table while inoculating.

ISOLATE #1 Results for "Isolate #1" ***Please fill out the table**** 1. Blood agar: 2. Nitrate Test: Test Results Interpretation Blood agar (type of hemolysis) Nitrate test 3. Gelatinase Activity: Gelatinase activity Resistant or Susceptible? Novobiocin Resistance Zone Diameter: 4. Novobiocin Resistance: 5. Coagulase Test: Coagulase (Sure-vue test) 1. Based on your results, what is the possible identification (Genus and species) of “Isolate #1"? I 9 10 11 12 3 14

My questions are in the picture

PLEASE answer the 2 with no much explanation Culture media is sterilized after the inoculation of microbes to ensure optimal growth of target microorganisms True False     Microwave oven available in the laboratory can be used to heat culture media, as well as food for lunch. True False

i need the answer quickly

Can you help me?

I need help with microbiology What is the magnification of each of the following objectives? scanning:   low power:   high dry:   oil immersion:

MATCHING TYPE. Match the phlebotomy materials found in Column A to the Collection Method found in Column B. Column A: Materials 1. Cotton 2. Plain glass tube3. Red top glass tube4. Gauge 23 syringe5. Two-way needle6. Adapter7. Lancet8. Lavender top plastic tube9. Tourniquet10. Micropore Column B: Collection MethodA. Syringe MethodB. Evacuated SystemC. Winged CollectionD. Capillary CollectionE. All of the aboveF. Syringe and Evacuated onlyG. Evacuated and Winged

Topic: Preparation of Microbial Suspension 5. Over-dilution with sterile water. Effect: Rationale:

Microbiology question. Chose the right answer

Microbiology question. Can you please choose the write answer and explain why it’s right and others are wrong.