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By: Brian Zaller
   Fast/inexpensive
    way to copy small
    segments of DNA
   “Amplifies”-Copies-
    Small segments of
    DNA
   Heralded as one of
    the most important
    scientific advances
    in molecular
    biology
   Mapping techniques in the Human Genome
    Project

   DNA fingerprinting

   Detection of bacteria and viruses

   Diagnostics of genetic disorders
1.    DNA sample is heated to separate it
2.    “Taq Polymerse” builds two new stands of
      DNA
3.    This results in a replica of the original DNA
4.    This process can be repeated 30-40 times
     ◦ Can create millions of copies of the original DNA

5.    This process is completed in a few hours
The Polymerase Chain Reaction
   Discovered in the 1980’s by Kary Mullis
    ◦ Won Nobel Peace Prize in Chemistry later because of PCR
   Started to get attention from scientist across
    America
   5000+ Scientific papers wrote about it
   Became commonly used to detect certain
    diseases
   Now commonly used in many medical research
    applications
    ◦ DNA cloning
    ◦ Diagnostics of hereditary diseases
    ◦ Identification of genetic fingerprinting
   HIV-1(Causes AID’s)
   Hepatitis B and C
   Human Papilloma Virus
   Chlamydia
   Neisseria Gonorreae
   Many other diseases
   May be used in predicative test methods for
    figuring out who is predisposed to common
    disorders such as:
    ◦ Heart Disease
    ◦ Cancer
In conclusion the Polymerase Chain Reaction is
a very helpful way to replicate DNA and
diagnose certain diseases. It is a very realizable
way to test and analyze the DNA and is also
very efficient in the sense that it only takes a
few hours.
"PCR Fact Sheet." PCR Fact Sheet. 27 Feb. 2012. Web. 23 May 2012.
       <http://www.genome.gov/10000207>.

"Applications of PCR." Applications of PCR. Roche. Web. 23 May 2012.
       <http://molecular.roche.com/About/pcr/Pages/Applicationsof
       PCR.aspx>.

 "History and Development of the Polymerase Chain Reaction (PCR)."
      History of PCR. Web. 23 May 2012.
      <http://www.molecularstation.com/pcr/history-of-pcr/>.

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PCR DNA Amplification Discovery and Applications

  • 2. Fast/inexpensive way to copy small segments of DNA  “Amplifies”-Copies- Small segments of DNA  Heralded as one of the most important scientific advances in molecular biology
  • 3. Mapping techniques in the Human Genome Project  DNA fingerprinting  Detection of bacteria and viruses  Diagnostics of genetic disorders
  • 4. 1. DNA sample is heated to separate it 2. “Taq Polymerse” builds two new stands of DNA 3. This results in a replica of the original DNA 4. This process can be repeated 30-40 times ◦ Can create millions of copies of the original DNA 5. This process is completed in a few hours
  • 6. Discovered in the 1980’s by Kary Mullis ◦ Won Nobel Peace Prize in Chemistry later because of PCR  Started to get attention from scientist across America  5000+ Scientific papers wrote about it  Became commonly used to detect certain diseases  Now commonly used in many medical research applications ◦ DNA cloning ◦ Diagnostics of hereditary diseases ◦ Identification of genetic fingerprinting
  • 7. HIV-1(Causes AID’s)  Hepatitis B and C  Human Papilloma Virus  Chlamydia  Neisseria Gonorreae  Many other diseases
  • 8. May be used in predicative test methods for figuring out who is predisposed to common disorders such as: ◦ Heart Disease ◦ Cancer
  • 9. In conclusion the Polymerase Chain Reaction is a very helpful way to replicate DNA and diagnose certain diseases. It is a very realizable way to test and analyze the DNA and is also very efficient in the sense that it only takes a few hours.
  • 10. "PCR Fact Sheet." PCR Fact Sheet. 27 Feb. 2012. Web. 23 May 2012. <http://www.genome.gov/10000207>. "Applications of PCR." Applications of PCR. Roche. Web. 23 May 2012. <http://molecular.roche.com/About/pcr/Pages/Applicationsof PCR.aspx>. "History and Development of the Polymerase Chain Reaction (PCR)." History of PCR. Web. 23 May 2012. <http://www.molecularstation.com/pcr/history-of-pcr/>.