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Experiment - people.vcu.edu
Experiment - people.vcu.edu

... solution to combat Cardiovascular disease is heart regeneration. Unlike humans, many lower vertebrates when injured, are able to regenerate limbs, appendages or internal organs. The Zebrafish is a perfect model organism to use for this study because they are one of the few organisms that possess the ...
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... • The high rates of rearrangements and low rates of point mutations make mtDNA essentially worthless for the restriction site-based reconstructions of intrafamilial phylogeny for which cpDNA is so well suited. • The occasional losses of mitochondrial genes and introns may also serve as useful marker ...
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... • Run until... sufficient data – The GridION system enables users to run an experiment until sufficient data has been collected to reach a predetermined experimental endpoint. ...
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DNA Mismatch Repair and Synonymous Codon Evolution in

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... Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. ...
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Transcription Translation

... Medium (agar) had 20 amino acids to supplement mutant’s growth even if 1 was missing. Plated these on specific medium to determine what supplements were missing from fungi ...
The Volvox glsA gene - Development
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... cloned the copy of Jordan that is responsible for the Gls phenotype of strain 22gls1, and that the DNA flanking Jordan in B3.4-1 represented a portion of the gls locus of interest. Genomic clones that hybridized with fragments isolated from B3.4-1 were tested for their ability to rescue the Gls phen ...
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... DNA sequences in the probe. This is shown by the competition assays in lanes 3-8. An excess of unlabeled oligonucleotide with the same sequence as the labeled probe (“self”) prevents formation of the complexes with labeled probe, whereas “nonspecific DNA” in the form of E. coli DNA does not compete ...
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... like Roger Kornberg, awarded the 2006 Nobel prize for Chemistry, who has painstakingly studied the micromechanics of transcription, we’re getting a much clearer picture of what happens inside the nucleus, and how the billions of metres of DNA in your body are converted into RNA by an enzyme called R ...
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... 1883 – Schimper – Independent binary fission of chloroplasts, and a resemblance of chloroplasts to cyanobacteria 1905 - Mereschkowsky – Endosymbiosis 1924 - Korshikov - Cyanophora paradoxa fossil described – transition organism 1959 - Stocking and Gifford - Independent DNA in chloroplasts 1970 – Mar ...
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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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