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Introduction To Polymerase Chain Reaction (PCR)
Introduction To Polymerase Chain Reaction (PCR)
Polymerase Chain
Reaction (PCR)
Review: The structure of
DNA
Unzipping
Antiparallel Strands
Review: Genome Sizes
Pine: 68 billion bp
Corn: 5.0 billion bp
Soybean: 1.1 billion bp
Human: 3.4 billion bp
Housefly: 900 million
bp
Rice: 400 million bp
E. coli: 4.6 million bp
HIV: 9.7 thousand bp
http://www.cbs.dtu.dk/databases/DOGS/abbr_table.txt
The Problem...
Identifying a 500bp
sequence in a genome would
be like finding a section of
this tape measure only 4 feet
long = 122 cm!
How many molecules do we
need to be able to see them?
To be visible on an agarose gel, need
around 10 ng DNA
For a 500-bp product band, weighing
660 g/mol.bp, therefore need 10 x 10-
9
/ (500*660) = 3.03x 10-14 moles
Avogadro’s number = 6.02 x 1023
Therefore need 1.8 x 1010 copies!
Denaturation: 30 - 60 sec
Annealing: 30 - 60 sec
Extension: 30 - 60 sec
Water
Buffer solution
DNA template
Primers
Nucleotides
Mg++ ions
DNA
Polymerase
PCR Reaction: Water
Water
The medium for all other
components.
PCR Reaction: Buffer
Buffer
Stabilizes the DNA polymerase,
DNA, and nucleotides
500 mM KCl
100 mM Tris-HCl, pH 8.3
Triton X-100 or Tween
PCR Reaction: Template DNA
DNA template
Contains region to
be amplified
Any DNA desired
Purity not
required
Should be free of
polymerase
inhibitors
PCR Reaction: Primers
Primers
Specific for ends of
amplified region
Forward and Reverse
Annealing temps
should be known
Depends on primer length,
GC content, etc.
Length 15-30 nt
Conc 0.1 – 1.0 µM (pMol/µL)
PCR Reaction: Nucleotides
Nucleotides
Added to the
growing chain
Activated NTP’s
dATP, dGTP, dCTP, dTTP
Stored at 10 mM, pH 7.0
Add to 20-200 µM in
assay
PCR Reaction: Magnesium
Mg++ ions
Essential
co-factor of DNA polymerase
Too little: Enzyme won’t
work.
Stabilizes the DNA double-
helix
Too much: DNA extra
stable, non-specific priming,
band smearing
Used at 0.5 to 3.5 µM in the
assay
PCR Reaction: Polymerase
DNA
Polymerase
The enzyme
that does the
extension
TAQ or similar
Heat-stable
Approx 1 U /
rxn
A Typical PCR Reaction
Component 1X 20X
Sterile Water 38.0 µL 760 ul
10X PCR Buffer 5.0 µL 100 µL
MgCl2 (50mM) 2.5 µL 50 µL
dNTP’s (10mM each) 1.0 µL 20 µL
PrimerFWD (25 pmol/ul) 1.0 µL 20 µL
PrimerREV 1.0 µL 20 µL
DNA Polymerase 0.5 µL 10 µL
DNA Template 1.0 µL --
Aliquot
Total Volume 50.0 µL 980 µL 49 µL
Add DNA
as last step
Typical Thermal Cycler
Conditions