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HotStarTaq® Plus DNA Polymerase and Master Mix and
HotStarTaq® Plus DNA Polymerase and Master Mix and

... QIAGEN PCR Buffer, dNTPs, and MgCl2. The kit is also supplied with CoralLoad Concentrate, which can be optionally added to the master mix prior to the start of PCR (Figure 3). With the HotStarTaq Plus Master Mix Kit, there is no need for separate pipetting of individual components, minimizing the ri ...
Natural Transfer of Conjugative Transposon Tn916 between Gram
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... The data presented in this report provide evidence that the streptococcal conjugative transposon Tn916 is able to cross naturally the barrier between a variety of gram-positive and gram-negative eubacteria, with subsequent expression in the new host. Although we did not make any attempt to determine ...
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CMSC 838T – Lecture 10 Genomics
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No Slide Title

... Rearrangement occurs at one allele at a time and continues until a productive rearrangement occurs. If both kappa alleles rearrange nonproductively, rearrangement will begin at the lambda locus. If all 4 alleles (both kappa alleles and both lambda alleles) rearrangements are nonproductive, the B cel ...
Brief Survey on DNA Sequence Mining
Brief Survey on DNA Sequence Mining

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Chapter 18: Altering the Genetic Message

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... Sections of the genome of the field isolate coding for the main surface glycoproteins of EHV-1 were selected for surveying the Prostejov field isolate and for determining the stability of the isolated virus during the passaging in the cell culture. These glycoproteins are crucial both for the proper ...
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Cross-dressing or Crossing-over: Sex Testing of Women Athletes

... • Purpose of meiosis: in animals, produce gametes with just half the parents’ genetic material. Gametes are ______ (haploid/diploid). • Mechanism: Only one of each pair of homologous chromosomes gets into each gamete. • The happy ending: Gametes from the two parents get to fuse, restoring the origin ...
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Chapter 4 Evolutionary Model of Immune Selection

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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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