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Genetic Tehcnology I - Fulton County Schools
Genetic Tehcnology I - Fulton County Schools

Genetic Engineering
Genetic Engineering

... This process may be divided into the following steps: ● Isolation of plasmid DNA containing the cloned sequence of interest. ● Digestion (cutting) of the plasmid into discrete fragments with restriction endonucleases. ● Separation of the fragments by agarose gel electrophoresis. ● Purification of th ...
Introduction_to_Enzymes (1)
Introduction_to_Enzymes (1)

... Almost all chemical reactions in an organism are controlled by enzymes. ...
DNA: Structure and Functions
DNA: Structure and Functions

I have.. Who has.. DNA produced from mRNA by reverse
I have.. Who has.. DNA produced from mRNA by reverse

... between DNA fragments by complementary base pairing ...
6.2 Recombinant DNA Technology
6.2 Recombinant DNA Technology

...  DNA extracted from human cells  DNA treated with restriction enzyme, cuts the DNA at specific sites, produce “sticky end”  Bacterial plasmid cut with same enzyme ...
Gene Technology
Gene Technology

Scientific Notebook
Scientific Notebook

... 16 weeks, three hour lab meeting/week (either one 3-hour meeting or three 1-hour meeting) A total of 48 hours of lab time Each lab activity should be assigned as a reading assignment prior to the class meeting. Activities may require adjustment to meet the time limitations of a particular course. We ...
GENETICS
GENETICS

Notes_DNA Replication_teacher
Notes_DNA Replication_teacher

... the new DNA strand. This means that it must constantly back track to copy parts of the strand newly exposed by helicase. Since this process takes longer than the other strand, it is called the lagging strand. The Strand that does not need to do this is called the leading strand. The fragments that a ...
Enzyme Fundamental Concepts Enzymes are biological catalysts
Enzyme Fundamental Concepts Enzymes are biological catalysts

20 - Biotechnology
20 - Biotechnology

... to cut strands of DNA at specific locations (restriction sites)  Restriction Fragments: have at least 1 sticky end (single-stranded end)  DNA ligase: joins DNA fragments  Cloning vector: carries the DNA sequence to be cloned ...
Biotechnology
Biotechnology

Answers-to-examination-in-Gene-technology_20121020
Answers-to-examination-in-Gene-technology_20121020

... Change in the DNA sequence that do not cause any change in the amino acid sequence. e) A palindromic sequence: CTTTGA change to 5’-CTATAG-3’ or 5’-TTATAA-5 3’-GATATC-5’ 3’-AATATT-3’ f) The advantage is the possibility to regulate the transcription of the gene. If the gene product is toxic and harmfu ...
Biotech Overview
Biotech Overview

DNA Structure, Replication and Protein Synthesis
DNA Structure, Replication and Protein Synthesis

... Insert the most appropriate words in each of the following spaces:  A section of DNA that causes the production of a protein is called a ___________________. Sections of  DNA that do not code for a particular protein are called _____________________________. The  protein ____________________________ ...
Watson, Crick and Wilkins
Watson, Crick and Wilkins

... Holley, an organic chemist, was able to determine the structure of transfer RNA, the RNA which at one end attaches to a specific amino acid and at the other has a code complementary to that on the messenger RNA. ...
Biotech 06
Biotech 06

DNA and Protein Synthesis
DNA and Protein Synthesis

PLASMIDS AND RESTRICTION ENZYMES
PLASMIDS AND RESTRICTION ENZYMES

... lacking that plasmid, the bacteria will then become resistant to that specific antibiotic. In nature, conjugation occurs with a very low efficiency; that is, only a small percentage of bacteria in a population can take in plasmid DNA at any point in time. The presence of an antibiotic resistance gen ...
Genetic Engineering
Genetic Engineering

Genetic engineering – stepping stones
Genetic engineering – stepping stones

... Plasmid of bacterial DNA is cut open. Insulin gene is inserted. Altered plasmid is inserted into another bacterium. Assaying techniques are used to check new gene. Transgenic bacteria begin to produce insulin. Transgenic bacteria are cloned and cultured. Human insulin is produced in significant quan ...
TABLE 3–1 Some Common Types of Enzymes
TABLE 3–1 Some Common Types of Enzymes

Biotechnology
Biotechnology

Chapter 9 - FIU Faculty Websites
Chapter 9 - FIU Faculty Websites

... Complex with nonspecific DNA does not bind Mg2+ whereas complex with cognate DNA bind Mg2+ ...
< 1 ... 88 89 90 91 92 93 94 95 96 ... 101 >

Restriction enzyme

A restriction enzyme or restriction endonuclease is an enzyme that cuts DNA at or near specific recognition nucleotide sequences known as restriction sites. Restriction enzymes are commonly classified into three types, which differ in their structure and whether they cut their DNA substrate at their recognition site, or if the recognition and cleavage sites are separate from one another. To cut DNA, all restriction enzymes make two incisions, once through each sugar-phosphate backbone (i.e. each strand) of the DNA double helix.These enzymes are found in bacteria and archaea and provide a defense mechanism against invading viruses. Inside a prokaryote, the restriction enzymes selectively cut up foreign DNA in a process called restriction; while host DNA is protected by a modification enzyme (a methyltransferase) that modifies the prokaryotic DNA and blocks cleavage. Together, these two processes form the restriction modification system.Over 3000 restriction enzymes have been studied in detail, and more than 600 of these are available commercially. These enzymes are routinely used for DNA modification in laboratories, and are a vital tool in molecular cloning.
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