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Introduction to Vectors - Pascack Valley Regional School District
Introduction to Vectors - Pascack Valley Regional School District

... There are three commonly used types of vectors: 1) plasmid vectors (e.g., pUC plasmids); 2) bacteriophage vectors (e.g., phage ); and 3) phagemid vectors (e.g., pBlueScriptTM). Each has a different use, and there are many derivatives of these basic building blocks. In BRITE, you will be using plasm ...
Lecture #6 Date ______ - Pomp
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Prentice Hall Review PPT. Ch. 12
Prentice Hall Review PPT. Ch. 12

... code? Why or why not? How do the proteins made affect the type and function of cells? Cells do not make all of the proteins for which they have genes (DNA). The structure and function of each cell are determined by the types of proteins present. 2. Consider what you now know about genes and protein ...
Lynch Syndrome
Lynch Syndrome

... The human body is made of small living units called cells. Cells in the body contain millions of genes. Genes are the basic structural and functional units of heredity. ...
GeneXPlus Transfection of Plasmid DNA into BJ-5ta Cells
GeneXPlus Transfection of Plasmid DNA into BJ-5ta Cells

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... M. jalapa plants with deep crimson flowers and M. jalapa plants with yellow flowers were studied. Cross-pollinating these plants produced plants with deep red flowers only (F1 generation). These F1 plants were allowed to self-pollinate, and the resulting seeds produced 450 deep red and 160 yellow M. ...
Genomic DNA Extraction Kit INSTRUCTION MANUAL
Genomic DNA Extraction Kit INSTRUCTION MANUAL

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Unit 5 Review
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UNIT 1: Biology as the Science of Life
UNIT 1: Biology as the Science of Life

...  diagram the double helix model of DNA.  demonstrate the replication of DNA.  discuss the evidence for the fact that DNA codes for proteins.  demonstrate the events of transcription and translation.  explain the connection between the proteins produced by translation and the traits possessed by ...
supplementary materials
supplementary materials

... earlier ORFs used the microarray experiments done by Chu et al [8] are not included in the sequence files. In the set of the middle genes identified by using the expression data at 2 and 5 hours, the following ORFs are not included in the S. cerevisiae sequence file: ...
Genetic mapping RFLP: Restriction Fragment Length
Genetic mapping RFLP: Restriction Fragment Length

... – Find the difference between the RFLP markers of family members with the disease and family members not having the disease. – It is likely that the RFLP marker that consistently differ is on the gene responsible for the disease, since family members have more or less the same genetic characteristic ...
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BCM301 Food Biotechnology
BCM301 Food Biotechnology

... DNA, and why they are important in biotechnology. Compare blunt ends with sticky ends. Know the mechanism by which electrophoresis separates pieces of DNA. List and know the steps of DNA cloning. Know how vectors are used to transform bacteria, and know the methods of selecting for successfully tran ...
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English - iGEM 2016
English - iGEM 2016

Outcross mutant to polymorphic strain for mapping and gene identity
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... A research team was investigating the properties of a newly-discovered enzyme, the product of which was a valuable drug. This enzyme had been extracted from cells of a marine worm, found in the North Atlantic, where the temperature is always close to 5 °C. All the proteins of such animals are adapte ...
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... 2. Unlike popular misconceptions about people with green skin or extra body parts, a mutation is simply a change in the nucleotide sequence, or base pair sequence, of DNA. Most mutations are either neutral (they have no effect) or harmful, but occasionally mutations can actually cause a helpful chan ...
Lecture 22: Protein Engineering
Lecture 22: Protein Engineering

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Document
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... • Plasmid – small, circular, self-replicating piece of DNA – R plasmids – special – genes inserted ...
TOPIC: Applied Genetics AIM: What methods can be used to
TOPIC: Applied Genetics AIM: What methods can be used to

... years. Recently, though, Frank is showing signs of old age, and you realize that your friend's days are numbered. You can't bear the thought of living without her, so you contact a biotechnology company that advertises pet cloning services. For a fee, this company will clone Frank using DNA from a s ...
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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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