Team:Newcastle/25 June 2010

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{{Team:Newcastle/mainbanner}}
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'''Friday'''
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'''25 June 2010'''
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===Aims===
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==Aims==
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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.  
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.  
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==Equipment List==
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===Equipment List===
* Solutions/ enzymes for PCR protocol
* Solutions/ enzymes for PCR protocol
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* Thermocycler
* Thermocycler
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==Polymerase Chain Reaction protocol==
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===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 10:39, 11 August 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.

  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