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Random Priming - ltcconline.net
Random Priming - ltcconline.net

... Anneal with random hexamers Primer extend with DNA polymerase and labeled nucleotides Denature and hybridize ...
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... FlyCutTM XmaI is expressed and purified from E.coli that carries the recombinant XmaI gene. The molecular weight is 37.6 kDa, with the recognition site at C^CCGGG. The reaction is conducted for 5-10 minutes at 37oC, and heat-inactivated at 65oC for 20 minutes. This enzyme is not sensitive to dam or ...
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... identical to an original molecule or cell To "clone a gene" is to make many copies of it - for example, in a population of bacteria  Gene can be an exact copy of a natural gene  Gene can be an altered version of a natural gene  Recombinant DNA technology makes it possible ...
Photo-damaged DNA Repair Under Extreme Conditions
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... Ultraviolet light can damage DNA by forming cyclobutane pyrimidine dimer (CPD) lesions. The repair strategy catalyzed by photolyases involves photo-excitation of the flavin adenine dinucleotide (FAD) cofactor and transfer of an electron to the DNA lesion, which leads to dimer cleavage. This repair m ...
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... Figure 17.4 Why might two DNA fragments inadvertently be cloned into a single vactor when using this cloning strategy? Two fragments of DNA from the organism could anneal together, making a concatemer, which would still have the two appropriate ends to be accepted into the vector, because both sites ...
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Genetic Engineering

... molecules gene (X) of interest (the target DNA) is inserted into a plasmid vector . The target DNA may be a single fragment isolated from an agarose gel , or a mixture of many fragments from, for example, genomic DNA . If the target has been prepared by digestion with EcoRI, then the fragment can be ...
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Enzymes - Science Geek

... CA Standard Students know enzymes are proteins that catalyze biochemical reactions without altering the reaction equilibrium and the activities of enzymes depend on the temperature, ionic conditions, and the pH of the surroundings. ...
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Drosophila Melanogaster

... (2) Digest a restricton enzyme, e.g. EcoRI (3) Ligate the digested DNA ...
< 1 ... 90 91 92 93 94 95 96 97 98 ... 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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