Preview

Ciprofloxacin Lab Report

Better Essays
Open Document
Open Document
1069 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Ciprofloxacin Lab Report
Question: What antibiotics work best in preventing E. coli k12 from growing; amoxicillin, ampicillin, or ciprofloxacin?

Hypothesis: If ciprofloxacin, an antibiotic, is added to petri dishes covered in live bacteria and left to sit for four to six days in an incubator at 37 degrees Celsius, then the petri dishes containing ciprofloxacin will have the largest zone of inhibition out of all of the other antibiotics tested because research shows that ciprofloxacin in one of the strongest antibiotic currently being sold on the market. The chemical formulas for the three antibiotics that I am using are as follows:
Amoxicillin Chemical Formula: C16H19N3O5S
Ampicillin Chemical Formula: C16H19N3O4S
Ciprofloxacin Chemical Formula: C17H18FN3O3
Ampicillin
…show more content…
After introducing the bacteria to individual petri dishes, quickly place the lid back on to prevent any contamination.

2. Label the 18 Petri Dishes- Amoxicillin, Ampicillin, Ciprofloxacin, and Control. There should be four labels of each antibiotic and six controls. When doing the following steps, make sure you are by a Bunsen burner because the heat radiating will kill off any other bacteria in the air and prevent contamination of the experiment.
a. Keep the antibiotic disks refrigerated until ready for use.
b. After introducing the live cultures of bacteria to each of the 18 petri dishes, remove the antibiotics (amoxicillin, ampicillin, and ciprofloxacin) from the
…show more content…
Using a pair of clippers, remove individual disks of amoxicillin from the magazine and place them in the middle of each petri dish labeled ‘amoxicillin’.
d. Using a pair of clippers, remove individual disks of ampicillin from the magazine and place them in the middle of each petri dish labeled ‘ampicillin’.
e. Using a pair of clippers, remove individual disks of ciprofloxacin from the magazine and place them in the middle of each petri dish labeled ‘ciprofloxacin’.
f. Using a hole-puncher, punch out six disks of filter paper to use for your control.
g. Dip each of the six disks of filter paper in water, and place each individual disk in the middle of the petri dishes labeled “control”.
h. After placing each disk into individual petri dishes, quickly place the lid back on to prevent any contamination.

3. Place the petri dishes in an incubator for several days. [Remember to store the dishes upside down, so the bacterial growth remains undisturbed by any water droplets] -The incubator should be set to the ideal temperature of 37 Degrees Celsius.

4. Leave the bacteria to develop for 4 days, as this will give the cultures enough time to

You May Also Find These Documents Helpful

  • Satisfactory Essays

    Incubate cells at 37 °C. Change media every 48 h for NPC maintenance or see the specific details for individual…

    • 237 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    Nt1310 Unit 3 Pathogens

    • 643 Words
    • 3 Pages

    Now you are ready to start culturing. Start with one of your plates you can do both at the same time but to avoid making any errors I recommend just doing one at a time. Using aseptic technique take the tube containing the pathogen you have chosen and sterilize it. Next, take your sterile pipette (dropper) and pick up a small amount of your sampled pathogen. Using aseptic technique again flame the tube and close it, set aside till you are ready to use for the next plate. Open the lid of the first plate (I used the one labeled 1-5 first)…

    • 643 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    This experiment called for the use of 37ºC dry heat incubator with an incubation time of 24-48 hours. E.coli grows any where from 10ºC - 45ºC so changing the temperature to a slightly higher temperature could've caused the samples to activate antibacterial properties otherwise not activated by a lower temp. Also, the amount of incubation could be lengthen to see if that changes the…

    • 939 Words
    • 4 Pages
    Powerful Essays
  • Good Essays

    Examine agar plate for bacterial growth. It there is no colony growth, incubate an additional 24 hours. Be very careful to not remove the lids.…

    • 630 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Today you will perform a frequently used procedure called the Kirby-Bauer Antimicrobial Susceptibility test (disc diffusion technique). Each group will inoculate his/her own plate of Mueller-Hinton agar with an assigned culture. To that inoculated plate, you will then aseptically add sterile filter paper discs (using a disc dispenser), which contain a known concentration of antibiotics. As soon as the antibiotic discs touch the agar, the antibiotic will begin to diffuse into the surrounding agar. During incubation the bacteria you inoculated onto the agar…

    • 1106 Words
    • 5 Pages
    Good Essays
  • Powerful Essays

    2. Place 2 to 3 loopfuls of the liquid culture on the slide with a sterile loop.…

    • 2253 Words
    • 10 Pages
    Powerful Essays
  • Satisfactory Essays

    Finally, the agar plate is observed after 48 hours in the incubator. Data is recorded for each antibiotic by measuring, in millimeters, the cloudy space from the antibiotic disk, out. After data is recorded, the nutrient agar plate will be collected for safe disposal. Hands must be washed thoroughly with soap after handling bacteria…

    • 297 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Chem Lab.

    • 520 Words
    • 3 Pages

    10. Store the vial in the beaker provided so the vial remains in an upright position.…

    • 520 Words
    • 3 Pages
    Good Essays
  • Better Essays

    pGLO Lab Report

    • 835 Words
    • 4 Pages

    If the transformed E. coli is mixed with the ampicillin resistance gene, it will be able to grow in the ampicillin plates, but the non-transformed E.coli will not.…

    • 835 Words
    • 4 Pages
    Better Essays
  • Powerful Essays

    Bio 103 Esiencelab1-7

    • 39625 Words
    • 159 Pages

    Always follow the instruc ons in your laboratory manual and these general rules: Lab prepara on…

    • 39625 Words
    • 159 Pages
    Powerful Essays
  • Good Essays

    MicroOrganism

    • 777 Words
    • 4 Pages

    2.) First place 5-8 loops of the bacteria onto the slide in a circular area and heat fix the bacteria…

    • 777 Words
    • 4 Pages
    Good Essays
  • Good Essays

    3. Place four to five filter papers in the petri dish and drip few drops of water on the strips, this will maintain moisture in the agar cushions. 4. Remove a Pasteur pipette from its container and attach a bulb to it. 5.…

    • 978 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Cherry Belle Lab

    • 769 Words
    • 4 Pages

    2. Get a paper towel, fold it, and wet it with 15 ml of water and put it into petri dish C.…

    • 769 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Bacteria Lab Write-Up

    • 740 Words
    • 2 Pages

    Procedure: We started this lab on May 12, 2014. Using a permanent marker on the bottom of the dish, we divided it into 4 sections. We labeled the sections, W (water), A (alcohol), S (soap), and HP (hydrogen peroxide). Then, we labeled the perimeter of our dish with our initials and class period. Kyra rubbed her fingers across the surface of the table for 30 seconds (you can also use the bottom of your shoes, the door knob, etc.) Then, Christine lifted the lid off of the petri dish so that Kyra could gently rub her finger across the entire surface of agar. We were careful not to puncture the agar. Then, we replaced the lid. We wet one disc in each liquid using the forceps (shaking excess liquid off disk), and then placed the disc on the agar in the middle of the appropriate section. Soon, we closed the lid. Afterwards, we turned the agar dish into our teacher for incubation.…

    • 740 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Five Second Rule

    • 550 Words
    • 3 Pages

    16) Open the top of the petri dish and take the swab in a zigzag pattern on the top of the nutrient agar. 17) Put the top of the petri dish back on and label type of food and time. 18) Change gloves. 19) Repeat steps 12-17 except pick up the bologna from the ground at 8 seconds. 20) Repeat all the steps above 4 more…

    • 550 Words
    • 3 Pages
    Good Essays