• Study Resource
  • Explore
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
DNA Technology Notes (13.1 &13.2)
DNA Technology Notes (13.1 &13.2)

...  Biologists use DNA technology to produce plants with many desirable traits.  Genetically engineered cotton resists insect infestation of the bolls.  Sweet-potato plants are resistant to a virus that could kill most of the African harvest.  Rice plants with increased iron and vitamins ...
Sample pages 1 PDF
Sample pages 1 PDF

... numerous deletion and duplication syndromes have been described that are too small to be detected under the microscope using conventional cytogenetic methods, such as G-banding. The molecular cytogenetic methods have expanded the possibilities for precise genetic diagnoses, which are extremely impor ...
Molecular and Immunological Methods
Molecular and Immunological Methods

...  Most are capable of managing multiple fluorophores simultaneously, allowing multiple amplicons to be probed in a multiplex assay (we’ll discuss this in more detail later).  All are also associated with sophisticated data management and analysis software, which makes data analysis easy, reliable a ...
Table of Contents
Table of Contents

Biotechnology: Applications of DNA Manipulation
Biotechnology: Applications of DNA Manipulation

... catalyze the cleavage of DNA into small fragments. • The enzymes cut the bonds between the 3 hydroxyl of one nucleotide, and the 5 phosphate of the next. • There are many such enzymes, each of which recognizes and cuts a specific sequence of bases, called a recognition sequence or restriction site ...
Meiosis and mitosis
Meiosis and mitosis

... of genes in a linear array ...
BB30055: Genes and genomes
BB30055: Genes and genomes

... .a single pair of PCR primers will produce different sized products for each of the different length microsatellites ...
GENETIC MUTATIONS - Manning's Science
GENETIC MUTATIONS - Manning's Science

High-Throughput Analysis of Foodborne Bacterial Genomic DNA
High-Throughput Analysis of Foodborne Bacterial Genomic DNA

Chromosomal Alterations - ReadingSample - Beck-Shop
Chromosomal Alterations - ReadingSample - Beck-Shop

... numerous deletion and duplication syndromes have been described that are too small to be detected under the microscope using conventional cytogenetic methods, such as G-banding. The molecular cytogenetic methods have expanded the possibilities for precise genetic diagnoses, which are extremely impor ...
A Protein - Cygnus Technologies
A Protein - Cygnus Technologies

RFLP Lab Report
RFLP Lab Report

... by restriction enzymes, “sticky” or “blunt” ends are formed. Sticky ends occur when singlestranded regions of the ends are complementary, and blunt ends occur when cut are opposite each other. The size of DNA fragments generated depends on the distance between recognition sites. Though RFLP analysis ...
lab9
lab9

Giant DNA Lab Manual.
Giant DNA Lab Manual.

... Later on in lab, you will be working through molecular biology problems on paper. In order to thoroughly understand these more complex problems we will work through some simpler problems using DNA models this week. ...
Ch_20
Ch_20

... Chapter 20: DNA Technology and Genomics 1. How is a gene cut out of a chromosome? 2. How is recombinant DNA cloned? 3. How are genomes of interest kept in a research lab? 4. How can we find a “gene of interest” in a genomic library? 5. What is cDNA & how is it made? 6. What is PCR & how is it used? ...
OB35
OB35

KOD -Plus
KOD -Plus

... including without limitation reporting the results of purchaser's activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patents require a separate license from Roche. Further i ...
Frequently Asked Questions (FAQ`s) Q1. What are chromosomes
Frequently Asked Questions (FAQ`s) Q1. What are chromosomes

... chromosomes. Named for its discoverer, Murray Barr. Q7. What is the significance of sex chromosomes? Ans: Sex chromosomes play a unique role in many biological processes and phenomena, including sex determination, epigenetic gene expression, the distribution of genes in the genome, genomic conflict, ...
Ch. 5: Presentation Slides
Ch. 5: Presentation Slides

Data Encryption Using DNA Sequences Based On Complementary
Data Encryption Using DNA Sequences Based On Complementary

introducing single molecule real-time (smrt
introducing single molecule real-time (smrt

Gibson Assembly™ – Building a Synthetic Biology Toolset
Gibson Assembly™ – Building a Synthetic Biology Toolset

... and assembled, starting from the digitized genome sequence, and transplanted into a Mycoplasma capricolum recipient cell to create new M. mycoides cells controlled only by the synthetic chromosome. The only DNA present in the cells is the designed synthetic DNA, including “watermark” sequences, and ...
XIXth INTERNATIONAL CONFERENCE OF GENETIC DAYS, 5th …
XIXth INTERNATIONAL CONFERENCE OF GENETIC DAYS, 5th …

DNA ppt notes 2015
DNA ppt notes 2015

...  DNA degraded to fragments only a few hundred base pairs in length can serve as effective templates for amplification.  Large numbers of copies of specific DNA sequences can be amplified simultaneously with multiplex PCR reactions.  Commercial kits are now available for easy PCR reaction setup an ...
Research Article Comparison of the efficiency of the DNA extraction
Research Article Comparison of the efficiency of the DNA extraction

... different plants. Oryza sativa, Nicotiana tabacum, Hibiscus esculentus, Populus alba and Pinus sylvestris are economically important plant species all around the globe and most of these are widely used in plant biotechnology research. These species were particularly chosen because of the great inter ...
< 1 ... 54 55 56 57 58 59 60 61 62 ... 222 >

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.
  • studyres.com © 2025
  • DMCA
  • Privacy
  • Terms
  • Report