Team:Newcastle/25 June 2010

From 2010.igem.org

(Difference between revisions)
(Polymerase Chain Reaction protocol)
Line 1: Line 1:
 +
{{Team:Newcastle/mainbanner}}
==Polymerase Chain Reaction protocol==
==Polymerase Chain Reaction protocol==

Revision as of 13:54, 12 July 2010

iGEM Homepage Newcastle University BacillaFilla Homepage Image Map

Polymerase Chain Reaction protocol

Polymerase chain reaction (PCR) is a technique used to amplify a single or few a copies of a piece of DNA generating thousands to millions of copies of a particular DNA sequence.

  1. To avoid contamination, wear gloves
  2. To achieve optimum results, always do everything on ice

A basic PCR set up requires several components and reagents.These components include:

  1. DNA template that contains the DNA region (target) to be amplified.
  2. Two primers that are complementary to the 3' (three prime) ends of each of the sense and anti-sense strand of the DNA target.
  3. Taq polymerase or another DNA polymerase with a temperature optimum at around 70 °C.
  4. Deoxynucleoside triphosphates, the building blocks from which the DNA polymerases synthesizes a new DNA strand.
  5. Buffer solution, providing a suitable chemical environment for optimum activity and stability of the DNA polymerase.
Fri-gel.png Newcastle gel 20100625.jpg