![Recombinant DNA](http://s1.studyres.com/store/data/014936216_1-1e92d239fa0c1dcd2c5fff742815e16a-300x300.png)
Recombinant DNA
... recognition sequences have been purified. In the lab they can be used to cut DNA samples from the same source. ...
... recognition sequences have been purified. In the lab they can be used to cut DNA samples from the same source. ...
Computer programs for the analysis and the management of DNA
... the original set of fragments against the new DNA construction. The main disadvantages are the time used to match a large set of fragments and the strong dependency upon the order by which the individual fragments are matched. Also, as our experience has shown, it sometimes happens that fragments ha ...
... the original set of fragments against the new DNA construction. The main disadvantages are the time used to match a large set of fragments and the strong dependency upon the order by which the individual fragments are matched. Also, as our experience has shown, it sometimes happens that fragments ha ...
Cells in culture.
... fragments serve as templates in their turn, and within a few cycles the predominant DNA is identical to the sequence bracketed by and including the two primers in the original template. Of the DNA put into the original reaction, only the sequence bracketed by the two primers is amplified because the ...
... fragments serve as templates in their turn, and within a few cycles the predominant DNA is identical to the sequence bracketed by and including the two primers in the original template. Of the DNA put into the original reaction, only the sequence bracketed by the two primers is amplified because the ...
Synthese der Oligonukleotide
... The design of biomolecules with defined structures and functions is an unreached goal. Today, we understand protein folding only incompletely. Also how catalysis is achieved is not jet fully understood. Synthetic enzyme mimics or designed proteins mimics are still inefficient catalysts in comparison ...
... The design of biomolecules with defined structures and functions is an unreached goal. Today, we understand protein folding only incompletely. Also how catalysis is achieved is not jet fully understood. Synthetic enzyme mimics or designed proteins mimics are still inefficient catalysts in comparison ...
sequence analysis of the 5` coi gene region from dama
... peformed on a MJ Research PTC-100 thermal cycler. Electrophoresis conditions and gel extraction After the completion of the PCR reaction, the samples were mixed with 10 µl of loading buffer (Glycerol 40%, Orange G 0.025%) and electrophoresed through an 1.5% agarose gel in SB conductive medium (10mM ...
... peformed on a MJ Research PTC-100 thermal cycler. Electrophoresis conditions and gel extraction After the completion of the PCR reaction, the samples were mixed with 10 µl of loading buffer (Glycerol 40%, Orange G 0.025%) and electrophoresed through an 1.5% agarose gel in SB conductive medium (10mM ...
Unit IX: Identification of a Gram
... prime causes of human dysentery, comprise four species and many serotypes. Serotypes within genera are organisms of similar biochemical characteristics that can most easily be differentiated by serological typing, testing of the unknown bacterium for reactivity to different antibodies specific to ea ...
... prime causes of human dysentery, comprise four species and many serotypes. Serotypes within genera are organisms of similar biochemical characteristics that can most easily be differentiated by serological typing, testing of the unknown bacterium for reactivity to different antibodies specific to ea ...
File
... PCR allows scientists to make billions of copies of pieces of DNA from extremely small quantities of DNA This depends on Taq polymerase which synthesizes DNA during replication Enzymes have an optimum temperature range that they function, and Taq polymerase is stable at much higher temperatures than ...
... PCR allows scientists to make billions of copies of pieces of DNA from extremely small quantities of DNA This depends on Taq polymerase which synthesizes DNA during replication Enzymes have an optimum temperature range that they function, and Taq polymerase is stable at much higher temperatures than ...
DNA databases Rape in the US Victims States with Offender Laws
... Some states have enhanced their DNA database laws to allow for the collection and comparison of DNA from people who are arrested for crimes. This means that even though a person has not been convicted of a crime, their DNA can be compared to profiles in the Forensic index. If an arrestee's profile m ...
... Some states have enhanced their DNA database laws to allow for the collection and comparison of DNA from people who are arrested for crimes. This means that even though a person has not been convicted of a crime, their DNA can be compared to profiles in the Forensic index. If an arrestee's profile m ...
Agarose gel electrophoresis
![](https://commons.wikimedia.org/wiki/Special:FilePath/DNAgel4wiki.png?width=300)
Agarose gel electrophoresis is a method of gel electrophoresis used in biochemistry, molecular biology, and clinical chemistry to separate a mixed population of DNA or proteins in a matrix of agarose. The proteins may be separated by charge and/or size (isoelectric focusing agarose electrophoresis is essentially size independent), and the DNA and RNA fragments by length. Biomolecules are separated by applying an electric field to move the charged molecules through an agarose matrix, and the biomolecules are separated by size in the agarose gel matrix.Agarose gels are easy to cast and are particularly suitable for separating DNA of size range most often encountered in laboratories, which accounts for the popularity of its use. The separated DNA may be viewed with stain, most commonly under UV light, and the DNA fragments can be extracted from the gel with relative ease. Most agarose gels used are between 0.7 - 2% dissolved in a suitable electrophoresis buffer.