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DNA I & II

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About the author

Student
Level
General public
Study
biology
School/University
Stony Brook...

About the document

Konstantin P.
Published date
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documents in English
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Type
presentations
Pages
2 pages
Level
General public
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  1. Introduction
    1. DNA manipulation
    2. Procedure followed
  2. Written results
  3. Discussion
  4. References

DNA technology is vital to our technological progress as a society. Without such things as gene therapy which is part of DNA technology many medical feats would not have been accomplished. DNA manipulation is used in many aspects of life, ranging from farms to hospitals and the gene cloning we attempted in our lab was but a precursor to all these great advances.

[...] As predicted the lighter DNA base pairs traveled further than the heavier, more positive, slow ones. The actual cut off points we hypothesized were a little off but not by too much. The EcoRI cut off at 2400 not at 2000 base pairs, the BglI cut off at 1700 and 1400 not at 1700 and 1000 and the mixture cut off at 1400 and 1600 not at 1000 and 2000. These results could be explained by one of two reasons, either the time constraints and slight human error did not allow for the gel to run its path all the way out, the blurry picture also did not help the cause. [...]


[...] DNA I & II Introduction DNA technology is vital to our technological progress as a society. Without such things as gene therapy which is part of DNA technology many medical feats would not have been accomplished. DNA manipulation is used in many aspects of life, ranging from farms to hospitals and the gene cloning we attempted in our lab was but a precursor to all these great advances. The DNA manipulation can lead to many advances and understanding how DNA works is important not only for the scientist but also for the general public. [...]

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