1 / 8

Polymerase Chain Reactions (PCR): “Molecular Photocopying”

Polymerase Chain Reactions (PCR): “Molecular Photocopying”. A fast, inexpensive, and simple way to amplify (make lots of copies of) a small sample of DNA- invented in 1985 Inventor (Kary Mullis) was awarded Nobel Prize in Chemistry in 1993

macy
Télécharger la présentation

Polymerase Chain Reactions (PCR): “Molecular Photocopying”

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Polymerase Chain Reactions (PCR):“Molecular Photocopying” • A fast, inexpensive, and simple way to amplify (make lots of copies of) a small sample of DNA- invented in 1985 • Inventor (Kary Mullis) was awarded Nobel Prize in Chemistry in 1993 • Used for Human Genome Project, DNA fingerprinting, diagnosis of genetic disorders, etc.

  2. 1.Add Target DNA to a test tube which has: DNA polymerase (TAQ*) Short oligonucleotide** primer Copies of the four nucleotides *TAQ- Thermus aquaticus , heat stable DNA polymerase (from hot springs, like Yellowstone) **A molecule usually composed of 25 or fewer nucleotides; used as a DNA synthesis primer

  3. Heat to 95ºC to denature DNA to single strands

  4. Cool to between 50º and 65 ºC to allow primers (synthetic sequences of DNA) to join to target site. To “anneal” is to form hydrogen bonds between primer and DNA

  5. Warm to 72ºC. Taq DNA Polymerase binds to the primers and selectively copies the target region with complimentary nucleotides.

  6. Warm to 95ºC again to separate newly formed and original DNA strands. Then, REPEAT! After 30 cycles (a few hours) one billion copies are attained!

  7. Some Animations • PCR: • http://www.sumanasinc.com/webcontent/anisamples/molecularbiology/pcr.html • http://learn.genetics.utah.edu/content/labs/pcr/

  8. PCR Dash • Timekeeper starts clock (3 minutes) • 95°C player cuts apart DNA template • TC gives template pieces to 55°C player • 55°C player matches complimentary primer to each strand and attaches them with tape • The TC takes the primed strands to the 72°C player • 72°C player matches the complimentary polymerase product to each DNA strand and tapes it to the primer • The TC then takes the finished double stranded products back to the 95°C player who denatures (cuts) them • The cycle is then repeated as many times as possible before time runs out!

More Related