Lab report for Experiment #2: Extraction Your Name: Name of TA: Lab Partner’s Name: Lab Section: Title: Experiment #2: Extraction Purpose: What is the purpose of this lab? In your OWN words! Observations: Weighed out 3.2568 grams of chemical mixture that was yellow in color. Dissolved dry chemicals in 38 ml CH2Cl2 with gentle heating. Poured the yellow solution into sep funnel. Added 10 ml CH2Cl2 to flask to rinse‚ poured solution into sep funnel. Added 15 ml 3 M
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Experiment title: Extraction of Bacteria Plasmid DNA and Analysis of extracted DNA Samples Objectives: 1) To study and understand the steps for extract bacteria plasmid DNA. 2) To measure the concentration and purity of extracted DNA by using spectrometric method and agarose gel electrophoresis method. 3) Determine the size of extracted DNA by using agarose gel electrophoresis method. Materials and Methods: (Refer to UDEE2124 lab manual from page
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IB Physics Lab: Finding Specific Heat Capacity of a Solid using Method of Mixtures | VISHWASHANTI GURUKUL Department of science-Physics Year: 2012-14 Level: HL | Name of candidate : ……………………………………………… Date: 08/01/2013 Name of Teacher: Chandra Sekhar Mogilisetti “Professor Lieber notes that using copper in the manufacture of coffee cups is not the wisest choice.” Specific Heat Capacity of Solid
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DNA fingerprinting is a way of identifying a specific individual‚ rather than simply identifying a species or some particular trait. It is also known as genetic fingerprinting or DNA profiling. As a technology‚ it has been around since at least 1985‚ when it was announced by its inventor‚ Sir Alec Jeffreys. DNA fingerprinting is currently used both for identifying paternity or maternity and for identifying criminals or victims. There is discussion of using DNA fingerprinting as a sort of personal
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Magenta Psychological Statistics Abstract This paper will review different styles of research design along with how different variables within research can be measured. Statistics Research Question: Within the realms of a psychological statistics class‚ does blended course-delivery format result in students attaining a higher grade point average when compared to face-to-face and online delivery formats? Null Hypothesis: Within the realms of a psychological statistics class‚ blended
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Forensic DNA Evidence DNA has become one of the most accurate tools used in law enforcement in determining guilt or innocence. DNA is different in all people it is our “genetic blueprint.” DNA is so significant to law enforcement because DNA left at a crime scene can be collected and tested to see if there is a match. It is unique because it ensures accuracy and fairness. The initial use of DNA began in Britain in 1986; the FBI used it for the first time in the United States two years
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DNA COMPUTING ……. The future of Computing By Priya Parmar Paromita Bhattacharyya email: priya.parmar2389@gmail.com email:tan389@gmail.com contact no: 9820154325 contact no:9967585813
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DNA Packaging: Nucleosomes and Chromatin By: Anthony T. Annunziato‚ Ph.D. (Biology Department‚ Boston College) © 2008 Nature Education Citation: Annunziato‚ A. (2008) DNA packaging: Nucleosomes and chromatin. Nature Education 1(1) Each of us has enough DNA to reach from here to the sun and back‚ more than 300 times. How is all of that DNA packaged so tightly into chromosomes and squeezed into a tiny nucleus? The haploid human genome contains approximately 3 billion base pairs of DNA packaged
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This lab must be typed. Title DNA Fingerprinting Purpose Why are we doing this lab Background 1. What are restriction enzymes 2. When added to a DNA sample‚ what do restriction enzymes do 3. What do you call the specific sequence of bases the enzyme is searching for 4. What is a restriction digestion 5. What is the purpose of the water bath 6. The electrophoresis apparatus creates an electrical field with positive and negative poles at the ends of the gel. DNA molecules are negatively charged.
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will finish off talking about PCR‚ and then we will discuss how it can be used. If we go back to the slide of the double stranded DNA‚ and if we take that to a high temperature‚ the two strands separate‚ you then add the primers‚ which interact with ? On the strand‚ synthesis takes place in the 5-3 direction‚ then you end up with 2 molecules identical to the DNA‚ and then you do another round‚ so it’s an exponential increase. There are different enzymes and polymerases‚ which come from bacteria
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