Agarose Gel Electrophoresis

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The purpose of this experiment was to replicate DNA by using Polymerase chain reaction by observing and analyzing it by agarose gel electrophoresis
Genetic transformation is defined as the process where by a plasmid is introduced into a cell such that when the cell reproduces, it also makes a new copy of the plasmid. Plasmid is defined as a circular DNA particle that is within a microorganism and has a replicating quality that are autonomous. Escherichia coli, is a bacterium that is commonly used for genetic transformation in the laboratory because the E. coli bacteria is a single-celled organism that contain multiple plasmids which are commonly used for such process (Marcus 2018). As the bacteria repeatedly increase in population size, the overall number of plasmids also multiply because the plasmid contains its own replication originally. This new DNA that is introduced can also replicate freely based on the original bacteria chromosome. Genes of variable traits that benefit the organism are contained in the Plasmid DNA. For a culture of only transformed plasmids, there is a need for the organism to only keep the transformed plasmid. This transformed plasmid has genes that codes for protein which protects the cell from
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Large fragments of DNA move slower whiles small fragments will move faster. Since DNA is negatively charged, it tends to move towards the positive direction. “Increased attraction by the magnetic force also allows lighter molecules to travel faster.” (Serwer 1983). Since the gel box is polarized, the molecules migrate from one end to the positive side when electricity is pumped through the box. This technique allows scientist to test, purify and compare the distance traveled by the size and can prove the absence or presence of genetic transformation in DNA fragments in molecular