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11_Lecture_Presentation
11_Lecture_Presentation

... expression in eukaryotes  Applying Your Knowledge For each of the following, determine whether an increase or decrease in the amount of gene product is expected – The mRNA fails to receive a poly-A tail during processing in the nucleus – The mRNA becomes more stable and lasts twice as long in the c ...
CENTRAL DOGMA AND GENE REGULATION
CENTRAL DOGMA AND GENE REGULATION

... d. Termination of the Growing Chain. The tRNA reaches one of the three stop codons in the mRNA. This signals the completion of translation. Ribosomes fall all and polypeptide goes to the golgi for packaging and delivery. Codon: the triplicate code found on mRNA that codes for each of the 20 amino ac ...
chapter 19 the organization and control of eukaryotic
chapter 19 the organization and control of eukaryotic

... Eukaryotic genes also have repressor proteins to inhibit expression of a gene.  Eukaryotic repressors can cause inhibition of gene expression by blocking the binding of activators to their control elements or to components of the transcription machinery or by turning off transcription even in the p ...
Document
Document

... How to distinguish foreign from native genes? SQ4: The GC content of Bacillus anthracis is 33.97%. By analysis of codon use, would it likely be easier to detect a foreign gene originating from Borrelia burgdorferi or from Mycobacterium tuberculosis? ...
"Polymerase Chain Reaction (PCR)". In: Encyclopedia of Life Sciences
"Polymerase Chain Reaction (PCR)". In: Encyclopedia of Life Sciences

... This technique involves using RNA rather than DNA as the template for amplification. The procedure is very similar to conventional PCR but includes an initial step in which a DNA copy of the RNA template is produced using the enzyme reverse transcriptase. This enzyme, which is of viral origin, is a ...
Sequence Alignment - UTK-EECS
Sequence Alignment - UTK-EECS

... prepared for theory group meeting on July 16, 2003 ...
SynCAM2a ΔPDZ Δ4.1B ΔPDZ - University of Oregon (SPUR)
SynCAM2a ΔPDZ Δ4.1B ΔPDZ - University of Oregon (SPUR)

Topic 2
Topic 2

SEQUENCE
SEQUENCE

... Examples: NCBI Protein, Refseq, RefSNP, UniGene, Homologene, ...
Genetic Fine Structure
Genetic Fine Structure

Creating Transgenic Mice
Creating Transgenic Mice

... Goals of this tutorial -To learn a few term related to genetically modified organisms -To understand the value of using genetically engineered organisms to study developmental biology -To learn the basic approaches about how transgenic mice are produced Genetically Modified Organisms Genetically mod ...
Chapter 15~ The Chromosomal Basis of Inheritance ______
Chapter 15~ The Chromosomal Basis of Inheritance ______

... – Duchenne muscular dystropy (MD) – hemophilia  X-inactivation: 2nd X chromosome in females condenses into a Barr body ...
Yeast DNA Prep (Quick) Formosa
Yeast DNA Prep (Quick) Formosa

... debris are then removed by centrifugation. Nucleic acids and similar materials are precipitated in the ethanol. The majority of this material is RNA, which is degraded into small pieces by the RNase A. Precipitation with PEG in high salt removes large molecules but leaves small ones in solution, sep ...
DNA - NIU Department of Biological Sciences
DNA - NIU Department of Biological Sciences

... Any change in the base sequence of a DNA molecule is a mutation. Mutation is a completely random process: any DNA base can be mutated, whether it is in a gene or not. Basic types: 1. base substitutions: convert one base into another, such as changing an A into a G. 2. Insertions or deletions of larg ...
MS Word File
MS Word File

... Eukaryotes TATA Box and CAAT box TATA box=AT rich sequence similar to –10; CAAT box=GGCCATTCT within 100 bases of start site ...
File
File

... 1. lactose binds to the repressor protein 2. It changes the shape (structure) of the repressor protein 3. This change stops the repressor protein binding to the operator 4. So RNA polymerase is able to bind to promoter 5. Z and Y are transcribed and the mRNA is made 6. As a result, the bacteria can ...
File
File

... A string of ribosomes carrying out multiple translation on the same mRNA strand is called a polyribosome ...
SCI 30 UA CH 2 Review Questions
SCI 30 UA CH 2 Review Questions

... 5. A pea plant with green pea pods is crossed with a pea plant with yellow pea pods. Both plants come from lines of pea plants that have only produced one colour of pod. All offspring from this cross develop green pea pods. ...
Genetic Fine Structure
Genetic Fine Structure

as a PDF
as a PDF

... Figure 2 Measure of the G1 arrest after g-irradiation. For each point, 36106 cells were plated in three petri dishes of 6 cm diameter with DMEM medium. After 24 h at 378C, cells were washed in PBS bu€er and irradiated (in PBS) at a dose of ®ve grays using a Co60 irradiator (15 grays/min). PBS was th ...
Pierce chapter 7
Pierce chapter 7

... Crossing over • If 2 genes are on the same chromosome, but far apart, crossing over can allow for recombination of gametes • Genes very far apart on the same chromosome will always be separated by crossing over, and are not considered to be linked ...
Product Manual Plant DNA Isolation Reagent
Product Manual Plant DNA Isolation Reagent

Chapter 7 – Linkage, Recombination, and
Chapter 7 – Linkage, Recombination, and

... Crossing over • If 2 genes are on the same chromosome, but far apart, crossing over can allow for recombination of gametes • Genes very far apart on the same chromosome will always be separated by crossing over, and are not considered to be linked ...
File - Down the Rabbit Hole
File - Down the Rabbit Hole

... Mutations are a result in a change in DNA sequence – A protein with a different AA sequence could be produced. – Germ Cell - If mutations occur in sex cells they may be passed on to the next generation. – Somatic- A mutation occurring only in body cells may be a problem for the individual but will n ...
DNA SEQUENCING AND GENE STRUCTURE
DNA SEQUENCING AND GENE STRUCTURE

... reaction conditions. The result is a clean break, releasing a fragment without hidden damages, which is required if the mobilities of the fragments are to be very closely correlated so that the bands will not blur. (The specificity need be only about a factor of ten for the sequence to be read unamb ...
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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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