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Team:Newcastle/25 June 2010
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| - | ==Polymerase Chain Reaction protocol== | + | '''Friday''' |
| + | |||
| + | ===Aims=== | ||
| + | The aim of today's Lab practice is to run the products of a PCR reaction on a gel to visualise the inserts and backbones as they separate due to difference in mass. | ||
| + | |||
| + | ===Equipment List=== | ||
| + | |||
| + | * Solutions/ enzymes for PCR protocol | ||
| + | * GoTaq polymerase | ||
| + | * Gloves | ||
| + | * Agarose gel | ||
| + | * Primers(Forward and Results) | ||
| + | * dNTPs | ||
| + | * Buffers | ||
| + | * Ice | ||
| + | * Sample DNA | ||
| + | * Thermocycler | ||
| + | |||
| + | ===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. | 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. | ||
Revision as of 14:09, 12 July 2010
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Friday
Aims
The aim of today's Lab practice is to run the products of a PCR reaction on a gel to visualise the inserts and backbones as they separate due to difference in mass.
Equipment List
- Solutions/ enzymes for PCR protocol
- GoTaq polymerase
- Gloves
- Agarose gel
- Primers(Forward and Results)
- dNTPs
- Buffers
- Ice
- Sample DNA
- Thermocycler
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.
- 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.
