Fergus - Introduction to PCR Flashcards
What is DNA cloning?
The isolation, purification and amplification of a specific DNA sequence
What is Taq polymerase?
A DNA polymerase that exists in an organism called thermos aquaticus
What are the two main steps of DNA cloning using a PCR based approach?
Design complimentary oligonucleotide primers
Amplify clone using Taq Polymerase
What is the first thing you must do when designing a PCR?
Decide on the sequence you want to amplify
What do you do after you have decided on the sequence you want to amplify?
Decide on suitable primers for this sequence
What do you do after deciding on your primers?
Denature the DNA
How and why do you denature the DNA?
By heating the reaction up to about 50-65 degrees Celsius
This breaks the hydrogen bonds between the two strands of DNA
Results in single strands of DNA
We can now anneal our primers to the single strands using the correct optimal annealing temperature
What do we do after annealing our primers?
We need to add our Taq polymerase
How do we add our Taq polymerase?
Increase heat up to 72 degrees (optimum temperature for Taq)
What does Taq do?
Taq extends the primers we have added (cloning our DNA)
What do we do after Taq has extended to give us clones?
We repeat this PCR to give us multiple clones
After 20 cycle repeats how many copies of the target gene will we have?
A million
What is PCR?
(5)
Polymerase chain reaction
Method of amplifying DNA sequences in vitro
Exponential DNA replication process
Based on thermostable DNA polymerase
Requires some knowledge of sequence to be amplified
Who invented PCR?
Kary Mullis
List the three steps in a PCR cycle
Denaturation
Annealing
Elongation
(These are repeated again and again)