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DNA History PPT - Mayfield City Schools
DNA History PPT - Mayfield City Schools

... Scientific History  The march to understanding that DNA is the genetic material T.H. Morgan (1908)  Frederick Griffith (1928)  Avery, McCarty & MacLeod (1944)  Hershey & Chase (1952)  Watson & Crick (1953)  Meselson & Stahl (1958) ...
Ch 18 - Quia
Ch 18 - Quia

... ESTs can identify genes that are expressed -They are generated by sequencing the ends of randomly selected cDNAs ESTs have identified 87,000 cDNAs in different human tissues -But how can 25,000 human genes encode three to four times as many proteins? -Alternative splicing yields different proteins w ...
Bacterial Genetics
Bacterial Genetics

... • Sometimes when lambda come out of the chromosome at the end of the lysogenic phase, it crosses over at the wrong point. This is very similar to the production of an F’ from an Hfr. • When this happens, a piece of the E. coli chromosome is incorporated into the lambda phage chromosome • These phage ...
Student Handout Hands-on Activity HIV Reverse Transcription and
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... to fight other infections and diseases. Acquired immunodeficiency syndrome (AIDS) occurs when a person’s immune system is severely compromised. Without treatment, most people with AIDS die. Fortunately, researchers have developed drugs to treat HIV infection. A combination therapy, or drug cockt ...
ORLANDO BIOLOGY ~ LESSON PLANS Competencies for 21st
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... Single DNA primer (3’ end near sequence of interest) is annealed to template DNA and extended with DNA polymerase. ...
HSA Practice Currence
HSA Practice Currence

... oil that is accidentally spilled into the ocean by tankers. However, scientists can insert a gene into the DNA of a bacterium to give it the ability to break down the oil. This technology is an example of A crossing-over B DNA replication C gene splicing D translation ...
7.344 Directed Evolution: Engineering Biocatalysts
7.344 Directed Evolution: Engineering Biocatalysts

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Chapter 17 Nucleotides, Nucleic Acids, and Heredity
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... the transmission of hereditary information took place in the nucleus, more specifically in structures called chromosomes. • The hereditary information was thought to reside in genes within the chromosomes. • Chemical analysis of nuclei showed chromosomes are made up largely of proteins called histon ...
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biologi eksam quetion summary

...  1.Trans gene can be inserted into an embrytotic stemcell. This cell can either be grown on a medium and then injected into a mother animal as an embryo, 2 or it can be injected into a blastocyst of normal genes.  In the first case, transgenic animals will result  In the second case, chimeras wil ...
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mapping within a gene

... • complementation test on T4 showed two things: • 2 mutants were in two different genes = trans configuration • 2 mutants on the same gene = cis configuration • complementation tests are also known as a cis-trans test • Benzer called any complementation group identified by this test = cistron • ofte ...
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... • A restriction enzyme (or restriction endonuclease) is an enzyme that cuts double-stranded DNA at specific sites that it recognizes. • The enzyme makes two incisions, one through each of the sugar-phosphate backbones (i.e., each strand) of the double helix without damaging the nitrogenous bases. ...
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AP Biology Final Exam Topics 2015

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... sequence. The result is a set of double-stranded DNA fragments with single-stranded ends, called "sticky ends." Sticky ends are not really sticky; however, the bases on the single stranded ends do easily form base pairs with the complementary bases on other DNA molecules. Thus, the sticky ends of DN ...
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... Based on the cloning and amplification of identified ORFs into homologous (ideally used for bacterial and yeast proteins) or sometimes heterologous systems (insect cells which result in post-translational modifications similar to mammalian cells). A fusion tag (short peptide or protein domain that i ...
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... method uses heat to separate DNA strands from each other. An enzyme from a heat-loving bacterium is used to replicate the DNA when the correct nucleotides are added to a PCR machine. The PCR machine can make millions of copies of DNA in a day. Scientists analyze bacterial, plant, animal, and human D ...
ch 19 gene expression in eukaryotes
ch 19 gene expression in eukaryotes

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... transcriptional repressors. When the hormone GA is absent the GRAS domain binds transcription factors, inactivating them. When GA is present the DELLA domain binds the protein GID1. This binding causes the DELLA protein to be tagged for degradation (using ubiquitination). With DELLA proteins degrade ...
Ch. 9: Presentation Slides
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... • In genetic engineering, the immediate goal of an experiment is to insert a particular fragment of chromosomal DNA into a plasmid or a viral DNA molecule • This is accomplished by breaking DNA molecules at specific sites and isolating particular DNA fragments • DNA fragments are usually obtained by ...
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Exam 2 Spring 2007 and key

... 44. Mutation that deletes a termination codon will result in the transcription/translation of a protein that A. is most likely non-functional B. that is longer in size C that is shorter in size D. A and B are correct E. A and D are correct 45. A mutation that adds a termination codon to the center o ...
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... 22. How can we determine the size of the fragments that are produced when we treat DNA from 2 individuals with the same restriction enzyme? 23. How can a DNA fragment containing a particular nucleotide sequence can be isolated and identified from a sample containing many different DNA fragments? 24. ...
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Cre-Lox recombination



In the field of genetics, Cre-Lox recombination is known as a site-specific recombinase technology, and is widely used to carry out deletions, insertions, translocations and inversions at specific sites in the DNA of cells. It allows the DNA modification to be targeted to a specific cell type or be triggered by a specific external stimulus. It is implemented both in eukaryotic and prokaryotic systems.The system consists of a single enzyme, Cre recombinase, that recombines a pair of short target sequences called the Lox sequences. This system can be implemented without inserting any extra supporting proteins or sequences. The Cre enzyme and the original Lox site called the LoxP sequence are derived from bacteriophage P1.Placing Lox sequences appropriately allows genes to be activated, repressed, or exchanged for other genes. At a DNA level many types of manipulations can be carried out. The activity of the Cre enzyme can be controlled so that it is expressed in a particular cell type or triggered by an external stimulus like a chemical signal or a heat shock. These targeted DNA changes are useful in cell lineage tracing and when mutants are lethal if expressed globally.The Cre-Lox system is very similar in action and in usage to the FLP-FRT recombination system.
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