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    BioLab3 DNA Structure and Function Lab Report Student Name: I. DNA Structure Define the following terms: Purines A colorless crystalline compound with basic properties‚ forming uric acid on oxidation. Pyrimidines A colorless crystalline compound with basic properties; a substituted derivative of this‚ especially the bases thymine and cytosine present in DNA. Nucleotides A compound consisting of a nucleoside linked to

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    DIFFERENCES BETWEEN PLASMID AND CHROMOSOMAL DNA IN BACTERIA. Eukaryotes have two or more chromosomes‚ prokaryotes such as bacteria possess a single chromosome composed of double-stranded DNA in a loop. DNA is located in the nucleoid of the cell and is not associated with protein A plasmid is an extra-chromosomal DNA molecule separate from the chromosomal DNA which is capable of replicating independently of the chromosomal DNA. Plasmids usually occur naturally in bacteria. A chromosome

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    the role of covalent bonds and hydrogen bonds in the structure of DNA. The role of covalent and hydrogen are as follows. hydrogen bonds‚ being easy to break‚ allow the DNA to break so that copies can be made. Whereas covalent bonds keep the sugar and phosphate together‚ which allows proper placement and structure. 3. Relate the role of the base pairing rules to the structure of DNA. The bases in a strand of DNA relate to the base pairing rule due to the combination of GC

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    Activity 1.3.1: DNA Detectives Introduction Bones can provide a snapshot of the identity of a person- they can predict height‚ stature‚ gender‚ ethnicity and even age. However‚ it is what lies inside these hard calcified tissues‚ the DNA housed inside the body’s cells‚ that holds the key to true genetic identity. Tissue is made up of many cells‚ the building blocks of life. Tucked inside the body’s cells‚ you will find chromosomes. These structures house your genes and contain the DNA code necessary

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    Objective: DNA is analyzed by agarose gel electrophoresis after being digested with EcoRI restriction endonucleasse. Procedures: λ DNA and puC18 DNA were put into two tubes respectively. Then‚ EcoRI buffer‚ EcoRI enzyme and deionized water would be put into both tubes. EcoRI enzyme was the restriction enzyme that cut the DNA at the specific sequence. The EcoRI buffer enhanced the stability of many enzymes and binds contaminants that may be present in DNA preparations. DI water was used to

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    ALU-HUMAN DNA TYPING THROUGH PCR Abstract This experiment is a qualitative experiment which shows if an individual has a specific dimorphic Alu element. We used a process called Polymerase Chain Reaction (PCR) to identify this Alu element. Introduction Knowing whether or not an individual possesses a certain gene can be very important in scientific research. Do to this importance PCR allows scientist to locate these Alu’s relatively easy. Our variables in this experiment were the hairs of

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    March 3‚ 2013 Wrongful convictions. | How the use of DNA can exonerate those wrongfully convicted. Imagine wasting years of your life in a jail cell on death row‚ for a crime you did not commit. You have to ask yourself “how could this happen? How did an innocent person get convicted if indeed they are innocent?” Those are just a few questions you think of when you think of wrongful convictions. Some questions can be answered by the common causes of wrongful convictions‚ such as‚ eyewitness

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    box in a class 2 promoter. He got a piece of DNA that had a good class 2 promoter and a piece of DNA that he knew he could cut with restriction endonucleases. The idea is to pair a piece of DNA with label on only one strand. In this case you want the label on the crick strand. You would take this piece of DNA with a hot phosphate on 5 prime end of the crick strand and denature it. The probe DNA helps you see where txn starts. You take that probe DNA and you mix it with transcript thats made by the

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    Utopia or Dystopia DNA PROFILING What is this? DNA profiling (also called DNA testing‚ DNA typing‚ or genetic fingerprinting) is a technique that is used to assist in the identification of individuals by their respective DNA profiles. DNA profiles are encrypted sets of letters that reflect a person ’s DNA makeup‚ which can also be used as the person ’s identifier. DNA profiling should not be confused with full genome sequencing. DNA profiling is used in‚ for example‚ parental testing and criminal

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    DATE: September 16‚ 2012 TO: Patricia Bennett‚ Supervising Principal FROM: Connor Sims‚ Associate SUBJECT: Oil Drilling & Gas Extraction Industry in the US Analysis (21111) This report presents information regarding the industry‚ the primary operator of oil and gas field properties. The industry fuels its key buyers‚ the Natural Gas Distribution (22121) and the Petroleum Refining (32411) industries‚ with crude oil and natural gas. The industry continuously battles

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