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Chapter 4 part I
Chapter 4 part I

... each) that are complementary to regions on opposite strands that flank the target DNA sequence which 3’OH pointed toward each other after annealing. • A template sequence in a DNA sample that lies between the primer binding sites (100-35,000 bp.) • A thermostable DNA polymerase that can withstand be ...
What`s New and Newly Recommended in the
What`s New and Newly Recommended in the

41. Specific terms of reference for the NCR for drug
41. Specific terms of reference for the NCR for drug

... of reference. In the specific terms of reference, the NRC tasks dedicated to each selected pathogen or group of pathogens are described. It aims to guarantee the knowledge, the know-how and the epidemiological surveillance expertise of each NRC. The tasks list is not exhaustive and can be modified i ...
Genetic Transcription & Translation Lecture PowerPoint
Genetic Transcription & Translation Lecture PowerPoint

... PowerPoints, video tutorials, sample assignments and course syllabi. New materials are continually being developed, so check back frequently, or follow us on Facebook (Science Prof Online) or Twitter (ScienceProfSPO) for updates. • Many SPO PowerPoints are available in a variety of formats, such as ...
Brooker Chapter 15
Brooker Chapter 15

... Eukaryotic organisms have many benefits from regulating their genes For example ...
DNA Sequencing - ILRI Research Computing
DNA Sequencing - ILRI Research Computing

... DNA, which can be produced from plasmid cloning vectors that contain the origin of replication from a single stranded bacteriophage such as M13 or fd. The primer is complementary to the region in the vector adjacent to the multiple cloning site. ...
microfluidic microarray assembly and its applications to
microfluidic microarray assembly and its applications to

Codon Bingo - TeacherWeb
Codon Bingo - TeacherWeb

... What are TWO differences between DNA structure & RNA structure? ...
Biopolymers
Biopolymers

... is that each base can only be paired with its “complementary” base: A with G, C with T. Note that the bases are joined by hydrogen bonds (discussed earlier). Base-pairing is the key to replication in DNA. Note that if it you could straighten out DNA, it would be about a mm (bacteria) to a cm (e.g. v ...
Mutations and Gene Regulation
Mutations and Gene Regulation

... • Cell differentiation is the way that cells become different from each other as they go through mitosis. • At first, all cells are the same and are not specialized. These cells are called stem cells. • As they grow and divide they become differentiated and specialized into heart cells, brain cells ...
Transcription Biology Review
Transcription Biology Review

... • Proteins that line up several amino acid contacts bind strongly to specific DNA sequences ...
Chapter 6 and 9 - Wando High School
Chapter 6 and 9 - Wando High School

... Translocation – a chromosomal mutation that occurs when a part of the chromosome breaks off and is added to another chromosome 20. _________________ is when homologous chromosomes do not separate properly during meiosis. This can lead to a gamete with an _____________________ or ____________________ ...
Grade 9 Science Unit #3: Reproduction and Human Development
Grade 9 Science Unit #3: Reproduction and Human Development

... information required to develop and function any living organism. DNA was discovered in 1869. In 1944, Oswald Avery and his colleagues confirmed that it was genetic material that would determine how traits were passed from one generation to the next. In 1953, Watson and Crick completed a model of th ...
Linked genes
Linked genes

... • Body color and wing size must usually be inherited together, and therefore be located on the same chromosome. • However – nonparental phenotypes were also produced, suggesting that body color and wing size genes are only partially linked genetically. (see p.278,279) ...
Efficient whole-genome DNA methylation analysis of the Human
Efficient whole-genome DNA methylation analysis of the Human

... differences in methylation have been observed in a wide variety of genomic contexts; for example, both within “classic” promoter-associated CpG islands and also in distal, non-CpG island regions [1, 2]. Establishing a method to broadly and efficiently survey DNA methylation patterns genome-wide is t ...
Manana Arabuli Grigol Robakidze University
Manana Arabuli Grigol Robakidze University

... In eukaryotes a great part of non-coding segments of DNA, at the first glance, serves no function, but as suggested, they might be in charge of regulating which genes become active. They “oversee” active processing of information in a nucleus. If we remember the differentiation of blastomeres during ...
Nucleic Acids and the RNA World
Nucleic Acids and the RNA World

... strand (where DNA is a double strand) • However, RNA can appear to be a double stranded helix during what is called a Hairpin • This is when the secondary structure of RNA loops and forms a double stranded “stem” ...
Chromosomal mutations
Chromosomal mutations

... Chromosome Structure DNA wrapped around histone proteins forming bead-like units or “nucleosomes” These are coiled forming a “super coil” which coils to form a “chromosome” ...
Transformation of the bacterium E. coli using a gene for green
Transformation of the bacterium E. coli using a gene for green

... which the genetic material carried by an individual cell is altered by incorporation of foreign (exogenous) DNA. This foreign DNA may be derived from unrelated species and even other kingdoms, such as bacteria, fungi, plants or animals, which would otherwise be inaccessible to an organism. Bacteria ...
Replication vs. Transcription vs. Translation
Replication vs. Transcription vs. Translation

... -We express our genes by using unique combinations of nucleotides to synthesize unique combinations of proteins ...
Introduction to Molecular Biology
Introduction to Molecular Biology

... DNA. All living organisms have common characteristics such as replication, nutrition, growing and interaction with their environment. An organism is composed of organs which perform specific functions. Organs are made of tissues which are composed of aggregation of cells that have similar functions. ...
Chromosome “theory” of inheritance
Chromosome “theory” of inheritance

... between chromosomes, and – within each chromosome – their order are both invariant. In other words, if we examine chr. 1 (by the way, they are numbered according to size, eXcept for the X), then in every human being, that chromosome will contain the exact same genes (note – I did not say the exact s ...
Isotype class switching is a biological mechanism that
Isotype class switching is a biological mechanism that

... chain constant region exons and allowing substitution of a γ, α or ε constant region gene segment. The free ends of the DNA are rejoined by a process called non-homologous end joining (NHEJ) to link the variabledomain exon to the desired downstream constant domain exon of the antibody-heavy chain. I ...
NBT Briefing - EcoNexus December 2015
NBT Briefing - EcoNexus December 2015

... component  can  recognise  a  specific  short  stretch  of  DNA  (9-­‐12  bases)  and  the  nuclease  (N)3   component  will  cut  the  DNA  at  that  site.  It  requires  two  ZFNs  –  each  to  dock  diagonally   across  the  doub ...
Table of Contents - Milan Area Schools
Table of Contents - Milan Area Schools

... non-target sites. • Bacillus thuringiensis bacteria produce a protein toxin that kills insect larvae pests and is 80,000 times more toxic than the typical chemical ...
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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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