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Genetics
Genetics

... • Transposons are small pieces of DNA that move readily from one site on bacterial chromosome to another or from bacterial chromosome to plasmid. • They carry antibiotic resistance genes. • Transfer of transposons on plasmids to other bacteria by conjugation contributes to antibiotic resistance. ...
Ch 20 GR
Ch 20 GR

Genetic Engineering
Genetic Engineering

Marktübersicht PCR-Kits
Marktübersicht PCR-Kits

... Heat inactivation: T4 DNA Ligase can be inactivated by incubation at 65 °C for 10 minutes. ...
(Pulse-field Gel Electrophoresis)
(Pulse-field Gel Electrophoresis)

1.3. Identity: Molecules and Cells Study Guide (Fisher)
1.3. Identity: Molecules and Cells Study Guide (Fisher)

1.3. Identity: Molecules and Cells Study Guide
1.3. Identity: Molecules and Cells Study Guide

... 1.3.d How can tools of molecular biology be used to compare the DNA of two individuals? DNA can be extracted from a person & then scientists can perform PCR (polymerase chain reactions) to amplify the DNA, making a sample millions of times bigger than the original sample. They can then cut the DNA w ...
DNA ppt
DNA ppt

Genetics
Genetics

... Relate the concept of the gene to the sequences of nucleotides in DNA Sequence the steps involving protein synthesis Categorize the different kinds of mutations that can occur in DNA Compare the effects of different kinds of mutations on cells and organisms. ...
DNA Structure and Function Notes
DNA Structure and Function Notes

... DNA is composed of two parallel strands of linked subunits (called nucleotides)  Nucleotides are made up of three parts: a phosphate group, a five-carbon sugar molecule, and a nitrogencontaining base. ...
DNA Structure and Function Video
DNA Structure and Function Video

... Providing you with an empty egg which could then be used  to place your iguana DNA in.  Now the NEW egg cell would  need to be placed into a reptile to help develop the egg  before being hatched.  After hatching you would get a baby  iguana that is an identical DNA match to the original iguana  you  ...
Please pass last week`s warm up to the aisle. HW # 63: Read and
Please pass last week`s warm up to the aisle. HW # 63: Read and

... •  Nobel Prize awarded in 1962 to 3 men: Watson, Crick and Wilkins but not to Rosalind Franklin who died of cancer at 37 getting the x ray data that provided the answers. ...
DNA stucture - worldofbiology09
DNA stucture - worldofbiology09

... DNA coils around histone proteins. 8 ball-shaped histone proteins and DNA forms a nucleosome. ...
Unit 3
Unit 3

... 27. Relate Mendel’s “law of independent assortment” to the behavior of chromosomes during meiosis; describe a situation in which the “law” of independent assortment would be violated. Breeding experiments allowed early geneticists to study and “map” genes, even though there was no way to “see” the g ...
DNA Analysis in China
DNA Analysis in China

... DNA Analysis in China by Hu Lan Genetics Laboratory, Institute of Forensic Sciences People’s Republic of China The Genetics Laboratory of the Institute of Forensic Sciences was the first DNA analysis unit established in China and is China’s central and main DNA profiling laboratory. The laboratory, ...
242413_Fx_DNA_Fingerprinting_Lab
242413_Fx_DNA_Fingerprinting_Lab

Last Name - JhaveriChemBioWiki
Last Name - JhaveriChemBioWiki

... 6. What part of DNA and RNA is the genetic information? What does the genetic information give instructions for making? ...
042310_recombinant_DNA2
042310_recombinant_DNA2

... copies could be generated) • A recognition sequence for a restriction enzyme (so that we can introduce our DNA of interest) • Reporter genes (to confirm we have successfully introduced the vector into the host cell) • Small size in comparison with host’s chromosomes (for easy manipulation) ...
Document
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... •DNA has a negative charge on its particles. • Molecules sort based on: •Charge - The greater the charge the more pull. •Size – Bigger pieces are slower, smaller are faster. •Shape - Coiled is slower straight is faster. •The negatively charged particles move toward the positive electrode while the p ...
Unit 1: Cells - Loudoun County Public Schools
Unit 1: Cells - Loudoun County Public Schools

... c) An amino acid change in a protein could affect its information, resulting in a change in the protein’s function. (Diabetes) d) The CHROMOSOMAL mutations are insertion, deletion, and substitution. Define and understand all. ...
Introduction
Introduction

MCB Lecture 4 – Genes and Chromosomes
MCB Lecture 4 – Genes and Chromosomes

Plasmid Miniprep - California State University
Plasmid Miniprep - California State University

ppt slides
ppt slides

... temperature resistant polymerase such as Taq polymerase, from Thermus aquaticus (a bacterium that lives in hot springs) • Taq polymerase extends the primers at temperatures up to 72˚C • When synthesis is complete, the whole mixture is heated further (to 95˚C) to melt the newly formed duplexes • Repe ...
How hair can reveal a history
How hair can reveal a history

... get one copy of each chromosome from our mother and one from our father, there are two numbers of repeats for each locus, which appear as peaks on an electropherogram, a chart produced by a genetic analyzer. The chance that two people have the same pairs at all 13 loci is astronomically low. It’s a ...
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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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