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Cloning Genes
Cloning Genes

... Restriction enzyme cuts the sugar-phosphate backbones at each arrow. ...
9-1
9-1

... Chemicals, computers, and bacteria are used to work with DNA. Scientists use these tools in genetics research and biotechnology. Restriction enzymes cut DNA. Restriction enzymes act as “molecular scissors.” 1)come from various types of bacteria 2)allow scientists to more easily study and manipulate ...
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... from a portion of the DNA molecule in the nucleus, and is the first step in gene expression. B. The second step, called translation, occurs when the mRNA leaves the nucleus of the cell and directs the production of a protein molecule. C. The Transcription Process 1. Transcription uses an enzyme call ...
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... Hypervariable Region 2. (See HVR1.) The limits of HVR2 are even more vague than for HVR1. HVR2 is generally said to start at location 1 and to extend for a few hundred bases, but part of this region is often called HVR3. ...
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Gel Electrophoresis
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Watson, Crick and Wilkins
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... • First they used repeat polymers such as UUUU… which produced PhePhePhe… • Next they used mixtures of known ratios of nucleotides to make the RNA: e.g., 3:1 U:G. • Thus P(UUU)= ¾* ¾ * ¾ , so 27 of every 64 triplets is UUU • P(UUG)= ¾ * ¾ * ¼, so 9 out of 64 triplets is two U’s and one G • P(UGG)= ¾ ...
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... A The DNA failed to replicate. B The deoxyribose sugar become separated from the DNA. C The genetic code change cause the wrong protein to form. D The RNA necessary to produce proteins was not present. 15. A student has cystic fibrosis, a genetic condition caused by the presence of a homozygous rece ...
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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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