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handout
handout

... 1) description of sequence of every gene valuable. Includes regulatory regions which help in understanding not only the molecular activities of the cell but also ways in which they are controlled. 2) identify & characterise important inheritable disease genes or bacterial genes (for industrial use) ...
Medical and Molecular Genetics
Medical and Molecular Genetics

... and segregation. At least three types of cis-acting elements are required including: origins (autonomously replicating sequences (ARS)), telomeres, and centromeres. Origins are the sites at which DNA replication is initiated on the chromosome and contain two functional sites: one, a specific segment ...
Genetics 3500 winter Test ii_ansers
Genetics 3500 winter Test ii_ansers

Chapter 8 Gene Transfer in Bacteria Conjugation Hfr Cells
Chapter 8 Gene Transfer in Bacteria Conjugation Hfr Cells

... • Can be transferred among bacterial species ...
Electrophoresis literally means “the condition of
Electrophoresis literally means “the condition of

... A segment of DNA has two restriction sites–I and II. When incubated with restriction enzymes I and II, three fragments will be formed–a, b, and c. Which of the following gels produced by electrophoresis would represent the separation and identity of these fragments? ...
Chapter 13 - Angelfire
Chapter 13 - Angelfire

... – Ex: a protein only cuts at AATT, it will cut the two fragments at different points - not across from each other (called sticky ends) • Called sticky ends because they want to bond with things due to their “open” end ...
recombinant dna and polymerase chain reactions
recombinant dna and polymerase chain reactions

... It is necessary to isolate the host bacteria that contain the gene that has been spliced as only want the recombinant DNA By having a gene on the same plasmid that gives resistance to an antibiotic, the other bacteria can be removed by culturing the bacteria in a medium that contains the antibiotic. ...
dna microinjection
dna microinjection

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figure 9-9
figure 9-9

... recombinant DNA molecule (Fig. 9–1): (1) restriction endonucleases recognize and cleave DNA at specific sequences to generate a set of smaller fragments. (2) the DNA fragment to be cloned is joined to a suitable cloning vector by using DNA ligases to link the DNA molecules together. 歐亞書局 ...
Biology 303 EXAM II 3/14/00 NAME
Biology 303 EXAM II 3/14/00 NAME

... did her father. Which of her parents underwent nondisjunction during meiosis, giving rise to the gamete responsible for the syndrome? ...
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HIV GENOTYPE ASSAY

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zChap11_140901 - Online Open Genetics
zChap11_140901 - Online Open Genetics

... fragments of DNA. The map is therefore made from physical entities (pieces of DNA) rather than abstract concepts such as the linkage frequencies and genes that make up a genetic map (Fig. 11.7). It is usually possible to correlate genetic and physical maps, for example by identifying the clone that ...
DNA to Protein - Duplin County Schools
DNA to Protein - Duplin County Schools

... http://www.classzone.com/cz/books/bio_07/resources/htmls/interactive_review/bio_intrev.html ...
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... Definition: two organisms that have similar ...
Introduction to high-‐throughput experiments and data analysis
Introduction to high-‐throughput experiments and data analysis

Biotechnology
Biotechnology

... Making Multiple Copies of a Gene or Other DNA Segment • To work directly with specific genes, scientists prepare well-defined DNA segments in multiple identical copies by a process called DNA cloning • Plasmids are small circular DNA molecules that replicate separately from the bacterial chromosome ...
Restriction Enzymes - Seattle Central College
Restriction Enzymes - Seattle Central College

... • Restriction enzymes are bacterial enzymes that cleave the sugar-phosphate backbone of the DNA at specific nucleotide. • They are member of the class of nucleases. Endonucleases cleave nucleic acid at internal positions, while exonucleases progressively digest from the ends of the nucleic acid mole ...
Extra Credit DNA Study Guide
Extra Credit DNA Study Guide

... 53. List in order the steps scientists need to do to add the gene to make insulin into bacteria. (pg 327-328). 1. Add a genetic marker such as a florescent protein tag or an antibiotic resistant tag. 2. Extract the insulin protein from the bacterial culture. 3. Transform the bacteria with the recomb ...
Zoo/Bot 3333
Zoo/Bot 3333

... blot analysis. The probe used in this instance hybridizes to a DNA fragment linked to the disease gene, which shows polymorphism for this restriction enzyme. The autoradiogram of this blot is shown above, aligned with the family pedigree. 5. In the above example, which of the following are likely t ...
Genetics 1
Genetics 1

... Heredity: is the study of the natural law or property of organisms whereby their offspring have various physical and mental traits of their parents or ancestors i.e. certain traits are transmitted from one generation to the next. Genetic information is carried on the DNA molecule as a gene. Gene: is ...
Filled in by Vector Core: Project: Received: Lot: BIOCENTER
Filled in by Vector Core: Project: Received: Lot: BIOCENTER

15 Guided Reading
15 Guided Reading

... - What techniques are used to study human DNA? Cutting DNA - Because DNA molecules are too large to analyze, what must scientists do first? ...
m10-expression
m10-expression

... Transcriptional measurements provide the ability to: Associate genes with biological processes / environmental conditions / stimuli / chemistry / regulation / etc. Diagnostic / prognostic biomarker for human (or other) sample outcomes. Microarrays were originally developed for sequencing. Array one ...
CH 16 and 17 PowerPoint
CH 16 and 17 PowerPoint

... • Uncertainties associated with gene tests for susceptibilities and complex conditions (e.g., heart disease, diabetes, and Alzheimer’s disease). • Fairness in access to advanced genomic technologies. • Conceptual and philosophical implications regarding human responsibility, free will vs genetic det ...
Gene cloning
Gene cloning

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Genomic library



A genomic library is a collection of the total genomic DNA from a single organism. The DNA is stored in a population of identical vectors, each containing a different insert of DNA. In order to construct a genomic library, the organism's DNA is extracted from cells and then digested with a restriction enzyme to cut the DNA into fragments of a specific size. The fragments are then inserted into the vector using DNA ligase. Next, the vector DNA can be taken up by a host organism - commonly a population of Escherichia coli or yeast - with each cell containing only one vector molecule. Using a host cell to carry the vector allows for easy amplification and retrieval of specific clones from the library for analysis.There are several kinds of vectors available with various insert capacities. Generally, libraries made from organisms with larger genomes require vectors featuring larger inserts, thereby fewer vector molecules are needed to make the library. Researchers can choose a vector also considering the ideal insert size to find a desired number of clones necessary for full genome coverage.Genomic libraries are commonly used for sequencing applications. They have played an important role in the whole genome sequencing of several organisms, including the human genome and several model organisms.
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