Team:Newcastle/25 June 2010
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- | [[Image:Newcastle gel 20100625.jpg|400px]] | + | =Polymerase Chain action 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. | ||
+ | # To avoid contamination, wear gloves | ||
+ | # To achieve optimum results, always do everything on ice | ||
+ | |||
+ | A basic PCR set up requires several components and reagents.These components include: | ||
+ | #DNA template that contains the DNA region (target) to be amplified. | ||
+ | #Two primers that are complementary to the 3' (three prime) ends of each of the sense and anti-sense strand of the DNA target. | ||
+ | #Taq polymerase or another DNA polymerase with a temperature optimum at around 70 °C. | ||
+ | #Deoxynucleoside triphosphates, the building blocks from which the DNA polymerases synthesizes a new DNA strand. | ||
+ | #Buffer solution, providing a suitable chemical environment for optimum activity and stability of the DNA polymerase. | ||
+ | |||
+ | [[Image:fri-gel.png|400px]] [[Image:Newcastle gel 20100625.jpg|400px]] |
Revision as of 13:44, 12 July 2010
Polymerase Chain action 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.
- To avoid contamination, wear gloves
- To achieve optimum results, always do everything on ice
A basic PCR set up requires several components and reagents.These components include:
- DNA template that contains the DNA region (target) to be amplified.
- Two primers that are complementary to the 3' (three prime) ends of each of the sense and anti-sense strand of the DNA target.
- Taq polymerase or another DNA polymerase with a temperature optimum at around 70 °C.
- Deoxynucleoside triphosphates, the building blocks from which the DNA polymerases synthesizes a new DNA strand.
- Buffer solution, providing a suitable chemical environment for optimum activity and stability of the DNA polymerase.