Personal Project: Book Review Blog - Phase 4 Searage Arabi 10A Supervisor: Miss Oznur Australian International Academy Tables of Contexts Introduction …………………………………………………………………………................….. Page 3. About My Personal Project ………………………………………………………………………. Page 3. Area Of Interaction (AOI) Used ………………………………………………………………… Page 4. Plan Layout ……………………………………………………………………………………………….Page 4. Summary …………………………………………………………………………………………………
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Course Guide School of Computing‚ Information and Mathematical Science/USP Library Faculty of Science‚ Technology and Environment The University of the South Pacific ii Produced by the University of the South Pacific‚ Suva‚ Fiji‚ 2013 First produced June 2010 Revised July 2012 Production team for semester 2‚ 2010 Course writers Colin Ash Paula Jones Deepak Bhartu Dinesh Kumar Kaylash Chaudhary Rajneel Totaram Rinel Ram Ronal Singh Shaveen Singh Sunil Lal Viren Sharma Valentine Hazelman
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In the 2nd phase‚ chitin will then be dissolved in less than 40% of Sodium Hydroxide‚ and heated to 90celcius which will convert the Chitin into Chitosan upon dissolving. The third phase will take place over 3 days. The nutrient broth and nutrient agar will be prepared first. On the 2nd day‚ the bacteria broth will be prepared prior to an overnight culture on the same day using E-Coli and M.Luteus. On the 3rd day‚ the Anti-bacterial well diffusion test will be carried out. Finally‚ we will
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Connor Lauffenburger 3/17/13 pGlo Transformation Lab Report I Introduction The purpose of this experiment was to show the genetic transformation of E. coli bacteria with a plasmid that codes for Green Fluorescent Protein (GFP) and contains a gene regulatory system that confers ampicillin resistance. A plasmid is a genetic structure in a cell that can replicate independently of chromosomes. In this lab‚ the Green Fluorescent Protein‚ which is typically found in the bioluminescent jellyfish Aequorea
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Agar.io is a addictive multiplayer action packed game developed by Matheus Valadares. In the game you are a cell and your goal is to gain as much mass as you can by consuming both pellets and smaller cells without being swallowed by bigger enemy cells. You can either play a deathmatch where everyone is the enemy‚ in a party with your friends or as a colored team that must consume other colors accept for your own. While playing the game‚ there is no set score‚ players have to respawn when all of
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Lab Session 8: Selective and Differential Media‚ Unknown ID (Enzyme Based Tests) Oct. 25-31st (To be turned in PRIOR to start of recitation for lab 8) Name: _____ ________ Objective: Analyze microbes from last week. Understand the use of antibiotics on microorganisms. Gain more knowledge about selective media and differential media. Practice use of the catalase test‚ coagulase and the oxidase test. Observe microbial flora of the nose. Significance: Understand the use of Mannitol
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were made and recorded each week to narrow down the scope of identification. Data has been presented in the tables‚ charts and drawings herein and reflect the results of microscopic observations as well as the differential tests results on various agars and broth cultures. Although all tests were not conclusive‚ the unknown organism labeled Unknown #11 was found to be a member of the family Enterobacteriacea and Genus Serratia marcescens. INTRODUCTION The field of Microbiology is the
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Kayleigh Schmidt Purpose 2: Exercise 1 Part A Purpose: The purpose of this lab is to explore inoculation‚ incubation‚ isolation‚ inspection‚ and identification. Inoculation is the placement of a small sample or cells or the material with cells on a culture media that helps these cells grow. Incubation involves the optimal growth temperature in a controlled setting and is when the cells start to become visible. There are two types of inspection‚ macroscopic and microscopic‚ and it helps to identify
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my thanks to the Principal of Western College of Commerce & Business Management‚ for extending his support. My deep sense of gratitude for providing Computer lab for completing 80 hrs. Thanks and appreciation to the people who supported for completing 40 hrs at the community level. I would also thank my Institution and my computer lab technician & attendant. I also extend my heartfelt thanks to my family and well wishers. Reason for joining Extension work Activity I have joined the department
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Objectives 1. To determine biochemical activities of microorganisms. 2. To observe the product of biochemical activities of microorganisms. 3. To learn the skills of inoculation agar tubes and agar plates. Introduction Microorganisms are able to carry out different biochemical activities with the ease of different enzymes. Each of these enzymes carries out one specific type of the chemical transformation. They convert substrates into product. A) Carbohydrates Fermentation Microorganisms utilize
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