"Petri dish" Essays and Research Papers

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    60 Petri Dish

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    The ten Petri dishes that exclusively did not contain an antibiotic in the bacteria culture served as the control. There were ten trials for the control and each level of IV. The experiment began by cleaning the work area and sterilizing it with 70% ethanol. Then trypticase soy agar (TSA) was poured into six groups of 60 Petri dishes (See Appendix 1). The dishes were labeled based on the antibiotic used and were left to dry and solidify at room temperature. After an hour‚ the dishes were placed in

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    Petri Dish Lab Report

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    tape Permanent marker Distilled water Graduated cylinder 3 petri dishes Lab spoons 3 beakers Sodium chloride 3 pipettes 3 grids Procedures: Day 1 Gather and prepare 3 petri dishes. Label each grid with the different percentage of salt in each solution (0.5%‚ 1.0%‚ 1.5%). Measure and cut 1 inch of one-sided tape. Stick the one sided tape on the side of the grid onto the back of a petri dish; repeat this for the other 2 petri dishes. Use the graduated cylinder and collect three 30-ml salt

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    Petri dish

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    - 3 Petri dishes prepared with agar - 1 disinfected swab - 1 bottle of disinfected water - A piece of filter paper - A hole puncher - 4 test tubes - 1 measuring cylinder - 1 pipette with disposable tips - Tetracycline - Clindamycin - Benzoyl peroxide - 1 beaker of water - P. acne bacteria culture - 1 forcep - 1 digital weighing scale - 1 marker pen 1. Before starting the experiment‚ make sure you clean your work area with Chlorox and wear gloves at all

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    Lab Report - Microbes Aim: To investigate four areas of the school and to find out which of the four have the most microbes. Areas to Sample: 1. Girl’s locker room (Senior school) 2. Girl’s locker room (Elementary school) 3. Boy’s locker room (Senior school) 4. Boy’s locker room (Elementary school) Hypothesis: We predict that the boy’s locker room in the senior school will have the most microbes. First of all‚ there are more people using our locker rooms in the Senior School

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    Petri Dish Lab

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    condition. The experiment starts with two petri dishes‚ and we filled each dish with fifty radish seeds. We made our first observations about the seeds that we see. We labeled one petri dish “Control‚” and the other was labeled “Experimental.” The experimental petri dish was put in the freezer for seven days‚ and the control petri dish was set on the counter in the normal-temp classroom for seven days as well. After those seven days‚ the experimental dish was removed from the freezer‚ and we used

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    My Favorite Dish

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    My Favorite Dish My favorite dish is one of the local foods in my hometown. It’s a kind of soup‚ but thicker than usual one. We can call it “Chicken Chowder Soup” in English. Because it is made from chicken soup‚ chicken’s visceral and some other batches such as eggs and shallot. The chicken soup is the most important part to make this dish delicious‚ because the soup is full of chicken’s delicate flavor. It’s easy to finish this dish‚ but it is really hard to make it well. My mother told me

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    Petri Dish Lab Report

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    to the plasmid. We then poured the cells onto four Petri dishes that contain Luria broth. Two of the Petri dishes contained the antibiotic‚

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    Dish Network

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    DISH NETWORK Headline Case Assignment Bus Strategy/Policy [Type the author name] 3/4/2014 [Type the abstract of the document here. The abstract is typically a short summary of the contents of the document. Type the abstract of the document here. The abstract is typically a short summary of the contents of the document.]   Should be in the present For example‚ a thorough SWOT analysis may help identify the challenges‚ and give insight as to reaction of the organization

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    liquid in and out several times‚ before depositing 3 drops onto the agar solution in a petri dish. Next‚ another group member used an alcohol wipe to sterilize the spore spreader. It was necessary to ensure no contamination of the spores. He then proceeded to distribute the spores around the dish and solution. After sealing the petri dish back up‚ I labeled the dish with our group name and date. Finally‚ the petri dish was placed inside of the culture dome to properly germinate. The second

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    Differential Staining

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    culture media and the uses for each‚ learn and employ the streak and pour dish techniques‚ and generate a pure culture of a specific organism. Set Up: For this experiment I needed: 1 Distilled water‚ 1 Paper towels‚ 1 10%-bleach or 70% alcohol solution‚ 1 Zip bag‚ 1 Pan to heat agar‚ 1 Isopropyl alcohol (rubbing alcohol)‚ 1 Cultures: S. epidermidis and L. acidophilus‚ 1 Gloves‚ Disposable‚ 1 Pencil‚ marking‚ 11 Petri dish‚ 60 mm‚ 2 Candles (flame source)‚ 1 Thermometer-in-cardboard-tube‚6 Test

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