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Lab - Recombinant DNA Simulation
Lab - Recombinant DNA Simulation

... Notice the EcoR1 cut sites are not directly across from each other on the DNA molecule. When EcoR1 makes its cuts, it leaves single-stranded “tails” on the new ends (see above). This type of end is called a STICKY END because complementary DNA sticky ends can be easily rejoined. In this activity, we ...
Transformations, Cloning
Transformations, Cloning

... Example of DNA sequencing noise. This base could have been an A or a G, but was read as A because it had a higher peak ...
Open File
Open File

... bases, by hydrogen bonds. Hydrogen bonds connect the complementary bases. The hydrogen bonds are represented by small circles. Color the hydrogen bonds grey or black. The DNA can actually "unzip" at the hydrogen bonds when it needs to replicate - or make a copy of itself. DNA needs to copy itself wh ...
5 Conclusion - Duke Computer Science
5 Conclusion - Duke Computer Science

Biol 207 Workshop 8 Answer Key
Biol 207 Workshop 8 Answer Key

... plasmid purification endonucleases sometimes cut the supercoiled circular plasmid producing the relaxed circular and linear forms of the DNA molecule. e) 1. A molecular biologist needs to be able to select for transformed bacteria. A plasmid with a selectable marker gene such as one that makes the b ...
VII. Molecular Biology Techniques
VII. Molecular Biology Techniques

... to measure relative amounts of the mRNA present in different samples. RNA (either total RNA or just mRNA) is separated by gel electrophoresis, usually an agarose gel. Because there are so many different RNA molecules on the gel, it usually appears as a smear rather than discrete bands. The RNA is tr ...
Chapter 12: Genetic Engineering
Chapter 12: Genetic Engineering

... Researchers have already developed tests for genetic disorders Researchers have also begun to look for genes that might predispose individuals to other medical problems, such as heart disease, diabetes, and cancer  If ...
Simulated Biodiversity Lab - ABC
Simulated Biodiversity Lab - ABC

Botana curus - ABC-MissAngelochsBiologyClass
Botana curus - ABC-MissAngelochsBiologyClass

Supramolecular Factories Inspired by Processive Enzymes
Supramolecular Factories Inspired by Processive Enzymes

... solution, as the chemical sequences of individual products are dependent on individual DNA template strands rather than the identity of other reagents present in solution. Therefore, large libraries of molecules can be synthesized by DTS in a single solution.7 Liu and coworkers synthesized a library ...
Chapter 04
Chapter 04

... • Sugar-phosphate forms double-helix ...
DNA and RNA Chapter 12-1
DNA and RNA Chapter 12-1

... http://www.mun.ca/biology/scarr/hersheychase-experiment.jpg ...
MyTaq™ HS DNA Polymerase
MyTaq™ HS DNA Polymerase

... tomato are used for agricultural research and are a ready source of DNA without causing too much damage to the main plant. The use of ISOLATE II and MyTaq means that high quality DNA can be extracted from many leaves and then used in PCR (fig. 1). Rice is a staple food for over half of the world’s p ...
Description
Description

... Methods of gene therapy:  Ex vivo/in vitro method: Cells are taken from the patients, cultured in the lab. This is followed by introduction of defective gene into somatic cells and modified cells are then administered to the patients. Example: this methods is useful to deliver the defective gene i ...
BIOTECHNOLOGY - Bishop Amat Memorial High School
BIOTECHNOLOGY - Bishop Amat Memorial High School

... How does DNA Fingerprinting Work?  When Restriction Fragments between individuals of the same species are compared, the fragments differ in length due to polymorphisms (slight differences in sequences).  Fragments are known as RFLP’s (Restriction Fragment Length Polymorphisms)  By using gel elec ...
BIG IDEA #2 - Science - Miami
BIG IDEA #2 - Science - Miami

...  Explain that every organism requires a set of instructions that specifies its traits and that genes located in chromosomes contain this hereditary information  Compare and contrast sexual reproduction requiring meiosis and asexual reproduction requiring mitosis and how they relate to heredity  D ...
different plant species - Bio
different plant species - Bio

... For example, Arabidopsis thaliana has a small diploid genome and correspondingly lower DNA yields. Nucleic acid yields from young plant tissues are often higher than from old plant tissue, because young plant tissue generally contains more cells than the same amount of older plant tissue. Young plan ...
Neutral DNA - Penn State University
Neutral DNA - Penn State University

... Genome-wide local alignment chains Human: 2.9 Gb assembly. Mask interspersed repeats, break into 300 segments of 10 Mb. ...
the DNA Binding Lab Lesson Plan Powerpoint
the DNA Binding Lab Lesson Plan Powerpoint

DNA Structure and history10
DNA Structure and history10

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Human Mitochondrial DNA
Human Mitochondrial DNA

REVIEW SHEET FOR GENETIC ENGINEERING AND TRANSGENICS
REVIEW SHEET FOR GENETIC ENGINEERING AND TRANSGENICS

... reduced the use and expense of harmful pesticides- engineer plants that are capable of degrading weedkillers (Roundup) so that crops are not harmed when spraying for weeds- improve nutrional value of crops (Golden Rice with beta-carotene)- extend the shelf life of produce (tomatoes, bananas)- Biorem ...
The Tools of Molecular Biology How do scientists make changes to
The Tools of Molecular Biology How do scientists make changes to

2013 Gen Tech Part 2
2013 Gen Tech Part 2

... The Tools of Molecular Biology How do scientists make changes to DNA? ...
Sex linked inheritance, sex linkage in Drosophila and man, XO, XY
Sex linked inheritance, sex linkage in Drosophila and man, XO, XY

... Fig: Alternative pairing possibilities for 5-bromouracil (5-BU). 5BU is an analog of thymine that can be mistakenly incorporated into DNA as a base. It has a bromine atom in place of the methyl group. (a) In its normal keto state, 5-BU mimics the pairing behavior of the thymine that it replaces, pai ...
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Comparative genomic hybridization



Comparative genomic hybridization is a molecular cytogenetic method for analysing copy number variations (CNVs) relative to ploidy level in the DNA of a test sample compared to a reference sample, without the need for culturing cells. The aim of this technique is to quickly and efficiently compare two genomic DNA samples arising from two sources, which are most often closely related, because it is suspected that they contain differences in terms of either gains or losses of either whole chromosomes or subchromosomal regions (a portion of a whole chromosome). This technique was originally developed for the evaluation of the differences between the chromosomal complements of solid tumor and normal tissue, and has an improved resoIution of 5-10 megabases compared to the more traditional cytogenetic analysis techniques of giemsa banding and fluorescence in situ hybridization (FISH) which are limited by the resolution of the microscope utilized.This is achieved through the use of competitive fluorescence in situ hybridization. In short, this involves the isolation of DNA from the two sources to be compared, most commonly a test and reference source, independent labelling of each DNA sample with a different fluorophores (fluorescent molecules) of different colours (usually red and green), denaturation of the DNA so that it is single stranded, and the hybridization of the two resultant samples in a 1:1 ratio to a normal metaphase spread of chromosomes, to which the labelled DNA samples will bind at their locus of origin. Using a fluorescence microscope and computer software, the differentially coloured fluorescent signals are then compared along the length of each chromosome for identification of chromosomal differences between the two sources. A higher intensity of the test sample colour in a specific region of a chromosome indicates the gain of material of that region in the corresponding source sample, while a higher intensity of the reference sample colour indicates the loss of material in the test sample in that specific region. A neutral colour (yellow when the fluorophore labels are red and green) indicates no difference between the two samples in that location.CGH is only able to detect unbalanced chromosomal abnormalities. This is because balanced chromosomal abnormalities such as reciprocal translocations, inversions or ring chromosomes do not affect copy number, which is what is detected by CGH technologies. CGH does, however, allow for the exploration of all 46 human chromosomes in single test and the discovery of deletions and duplications, even on the microscopic scale which may lead to the identification of candidate genes to be further explored by other cytological techniques.Through the use of DNA microarrays in conjunction with CGH techniques, the more specific form of array CGH (aCGH) has been developed, allowing for a locus-by-locus measure of CNV with increased resolution as low as 100 kilobases. This improved technique allows for the aetiology of known and unknown conditions to be discovered.
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