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Gene Cloning
Gene Cloning

... – For linear fragments rate of migration proportional to log10 molecular size ...
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lab 3 enzymes F09

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enzymes powerpoint - Pasadena High School

... Enzymes are highly specific—each one catalyzes only one chemical reaction.  Reactants are substrates: they bind to a specific site on the enzyme—the active site.  Specificity results from the exact 3-D shape and chemical properties of the active site. ...
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introduction to enzymes

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Learning objectives

... 1. Describe the natural function of restriction enzymes and explain how they are used in recombinant DNA technology. 2. Explain how the creation of sticky ends by restriction enzymes is useful in producing a recombinant DNA molecule. 3. Outline the procedures for cloning a eukaryotic gene in a bacte ...
Learning objectives
Learning objectives

... 1. Describe the natural function of restriction enzymes and explain how they are used in recombinant DNA technology. 2. Explain how the creation of sticky ends by restriction enzymes is useful in producing a recombinant DNA molecule. 3. Outline the procedures for cloning a eukaryotic gene in a bacte ...
PPT File
PPT File

... • DNA samples can be studied and compared by DNA fingerprinting • DNA is digested with restriction enzymes and then run on an agarose gel • When soaked in ethidium bromide, the DNA fragments can be seen directly under UV light • If greater sensitivity needed or if number of fragments would be too gr ...
< 1 ... 71 72 73 74 75 76 77 78 79 ... 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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